Canonical Allele Identifier: CA1923802152
Gene: NRG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.82856386_82856387delinsCT , CM000672.2:g.82856386_82856387delinsCT GRCh38
NC_000010.10:g.84616142_84616143delinsCT , CM000672.1:g.84616142_84616143delinsCT GRCh37
NC_000010.9:g.84606122_84606123delinsCT NCBI36
NG_013373.1:g.986073_986074delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372141.7:c.1028-9025_1028-9024delinsCT MANE Select ENSP00000361214.2:n.1028-9025_1028-9024delinsCT
ENST00000372141.6:c.1028-9025_1028-9024delinsCT ENSP00000361214.2:n.1028-9025_1028-9024delinsCT
ENST00000372142.6:c.365-9025_365-9024delinsCT ENSP00000361215.2:n.365-9025_365-9024delinsCT
ENST00000404547.5:c.1028-9025_1028-9024delinsCT ENSP00000384796.1:n.1028-9025_1028-9024delinsCT
ENST00000404576.6:c.440-9025_440-9024delinsCT ENSP00000385804.2:n.440-9025_440-9024delinsCT
ENST00000537893.1:c.-23-9025_-23-9024delinsCT ENSP00000440377.1:n.-23-9025_-23-9024delinsCT
ENST00000545131.5:c.-23-9025_-23-9024delinsCT ENSP00000441201.1:n.-23-9025_-23-9024delinsCT
ENST00000555784.5:c.340-2748_340-2747delinsCT ENSP00000451858.1:n.340-2748_340-2747delinsCT
ENST00000556918.5:c.518-9025_518-9024delinsCT ENSP00000451376.1:n.518-9025_518-9024delinsCT
ENST00000602794.5:c.*576-2748_*576-2747delinsCT ENSP00000473669.1:n.*576-2748_*576-2747delinsCT
NM_001010848.3:c.1028-9025_1028-9024delinsCT NP_001010848.2:n.1028-9025_1028-9024delinsCT
NM_001165972.1:c.1028-9028_1028-9027delinsCT NP_001159444.1:n.1028-9028_1028-9027delinsCT
NM_001165973.1:c.365-9025_365-9024delinsCT NP_001159445.1:n.365-9025_365-9024delinsCT
XM_005269444.3:c.1028-9025_1028-9024delinsCT XP_005269501.1:n.1028-9025_1028-9024delinsCT
XM_011539172.1:c.1028-9025_1028-9024delinsCT XP_011537474.1:n.1028-9025_1028-9024delinsCT
XM_011539173.1:c.1028-9028_1028-9027delinsCT XP_011537475.1:n.1028-9028_1028-9027delinsCT
XM_011539174.1:c.1028-95083_1028-95082delinsCT XP_011537476.1:n.1028-95083_1028-95082delinsCT
XM_011539175.1:c.1028-9025_1028-9024delinsCT XP_011537477.1:n.1028-9025_1028-9024delinsCT
XM_011539176.1:c.248-9025_248-9024delinsCT XP_011537478.1:n.248-9025_248-9024delinsCT
XM_011539177.1:c.248-9025_248-9024delinsCT XP_011537479.1:n.248-9025_248-9024delinsCT
XM_011539179.1:c.-20-9028_-20-9027delinsCT XP_011537481.1:n.-20-9028_-20-9027delinsCT
XM_005269444.5:c.1028-9025_1028-9024delinsCT XP_005269501.1:n.1028-9025_1028-9024delinsCT
XM_011539172.3:c.1028-9025_1028-9024delinsCT XP_011537474.1:n.1028-9025_1028-9024delinsCT
XM_011539173.3:c.1028-9028_1028-9027delinsCT XP_011537475.1:n.1028-9028_1028-9027delinsCT
XM_011539175.3:c.1028-9025_1028-9024delinsCT XP_011537477.1:n.1028-9025_1028-9024delinsCT
XM_017015573.2:c.1106-9025_1106-9024delinsCT XP_016871062.1:n.1106-9025_1106-9024delinsCT
XM_017015574.2:c.1106-9025_1106-9024delinsCT XP_016871063.1:n.1106-9025_1106-9024delinsCT
XM_017015575.2:c.1106-9028_1106-9027delinsCT XP_016871064.1:n.1106-9028_1106-9027delinsCT
XM_017015576.2:c.1106-9028_1106-9027delinsCT XP_016871065.1:n.1106-9028_1106-9027delinsCT
XM_017015577.2:c.1106-9025_1106-9024delinsCT XP_016871066.1:n.1106-9025_1106-9024delinsCT
XM_017015578.2:c.1106-9025_1106-9024delinsCT XP_016871067.1:n.1106-9025_1106-9024delinsCT
XM_017015579.2:c.1106-9028_1106-9027delinsCT XP_016871068.1:n.1106-9028_1106-9027delinsCT
XM_017015580.2:c.1106-9028_1106-9027delinsCT XP_016871069.1:n.1106-9028_1106-9027delinsCT
XM_017015581.2:c.1028-9028_1028-9027delinsCT XP_016871070.1:n.1028-9028_1028-9027delinsCT
XM_017015582.1:c.248-9025_248-9024delinsCT XP_016871071.1:n.248-9025_248-9024delinsCT
XM_017015583.1:c.248-9025_248-9024delinsCT XP_016871072.1:n.248-9025_248-9024delinsCT
XM_024447781.1:c.-20-9028_-20-9027delinsCT XP_024303549.1:n.-20-9028_-20-9027delinsCT
XR_001747009.2:n.1257-9025_1257-9024delinsCT
NM_001010848.4:c.1028-9025_1028-9024delinsCT MANE Select NP_001010848.2:n.1028-9025_1028-9024delinsCT
NM_001370081.1:c.1028-9028_1028-9027delinsCT NP_001357010.1:n.1028-9028_1028-9027delinsCT
NM_001370082.1:c.461-9025_461-9024delinsCT NP_001357011.1:n.461-9025_461-9024delinsCT
NM_001370084.1:c.1028-9025_1028-9024delinsCT NP_001357013.1:n.1028-9025_1028-9024delinsCT
NR_163251.1:n.1379-9028_1379-9027delinsCT
NR_163252.1:n.614-9028_614-9027delinsCT
NR_163253.1:n.1015-2748_1015-2747delinsCT
NM_001165973.2:c.365-9025_365-9024delinsCT NP_001159445.1:n.365-9025_365-9024delinsCT