Canonical Allele Identifier: CA1923802017

Gene: NRG3

Linked Data

• dbSNP Id: rs2063789895

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.82856121_82856123del , CM000672.2:g.82856121_82856123del	GRCh38
NC_000010.10:g.84615877_84615879del , CM000672.1:g.84615877_84615879del	GRCh37
NC_000010.9:g.84605857_84605859del	NCBI36
NG_013373.1:g.985808_985810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372141.7:c.1028-9290_1028-9288del MANE Select	ENSP00000361214.2:n.1028-9290_1028-9288del
ENST00000372141.6:c.1028-9290_1028-9288del	ENSP00000361214.2:n.1028-9290_1028-9288del
ENST00000372142.6:c.365-9290_365-9288del	ENSP00000361215.2:n.365-9290_365-9288del
ENST00000404547.5:c.1028-9290_1028-9288del	ENSP00000384796.1:n.1028-9290_1028-9288del
ENST00000404576.6:c.440-9290_440-9288del	ENSP00000385804.2:n.440-9290_440-9288del
ENST00000537893.1:c.-23-9290_-23-9288del	ENSP00000440377.1:n.-23-9290_-23-9288del
ENST00000545131.5:c.-23-9290_-23-9288del	ENSP00000441201.1:n.-23-9290_-23-9288del
ENST00000555784.5:c.340-3013_340-3011del	ENSP00000451858.1:n.340-3013_340-3011del
ENST00000556918.5:c.518-9290_518-9288del	ENSP00000451376.1:n.518-9290_518-9288del
ENST00000602794.5:c.*576-3013_*576-3011del	ENSP00000473669.1:n.*576-3013_*576-3011del
NM_001010848.3:c.1028-9290_1028-9288del	NP_001010848.2:n.1028-9290_1028-9288del
NM_001165972.1:c.1028-9293_1028-9291del	NP_001159444.1:n.1028-9293_1028-9291del
NM_001165973.1:c.365-9290_365-9288del	NP_001159445.1:n.365-9290_365-9288del
XM_005269444.3:c.1028-9290_1028-9288del	XP_005269501.1:n.1028-9290_1028-9288del
XM_011539172.1:c.1028-9290_1028-9288del	XP_011537474.1:n.1028-9290_1028-9288del
XM_011539173.1:c.1028-9293_1028-9291del	XP_011537475.1:n.1028-9293_1028-9291del
XM_011539174.1:c.1028-95348_1028-95346del	XP_011537476.1:n.1028-95348_1028-95346del
XM_011539175.1:c.1028-9290_1028-9288del	XP_011537477.1:n.1028-9290_1028-9288del
XM_011539176.1:c.248-9290_248-9288del	XP_011537478.1:n.248-9290_248-9288del
XM_011539177.1:c.248-9290_248-9288del	XP_011537479.1:n.248-9290_248-9288del
XM_011539179.1:c.-20-9293_-20-9291del	XP_011537481.1:n.-20-9293_-20-9291del
XM_005269444.5:c.1028-9290_1028-9288del	XP_005269501.1:n.1028-9290_1028-9288del
XM_011539172.3:c.1028-9290_1028-9288del	XP_011537474.1:n.1028-9290_1028-9288del
XM_011539173.3:c.1028-9293_1028-9291del	XP_011537475.1:n.1028-9293_1028-9291del
XM_011539175.3:c.1028-9290_1028-9288del	XP_011537477.1:n.1028-9290_1028-9288del
XM_017015573.2:c.1106-9290_1106-9288del	XP_016871062.1:n.1106-9290_1106-9288del
XM_017015574.2:c.1106-9290_1106-9288del	XP_016871063.1:n.1106-9290_1106-9288del
XM_017015575.2:c.1106-9293_1106-9291del	XP_016871064.1:n.1106-9293_1106-9291del
XM_017015576.2:c.1106-9293_1106-9291del	XP_016871065.1:n.1106-9293_1106-9291del
XM_017015577.2:c.1106-9290_1106-9288del	XP_016871066.1:n.1106-9290_1106-9288del
XM_017015578.2:c.1106-9290_1106-9288del	XP_016871067.1:n.1106-9290_1106-9288del
XM_017015579.2:c.1106-9293_1106-9291del	XP_016871068.1:n.1106-9293_1106-9291del
XM_017015580.2:c.1106-9293_1106-9291del	XP_016871069.1:n.1106-9293_1106-9291del
XM_017015581.2:c.1028-9293_1028-9291del	XP_016871070.1:n.1028-9293_1028-9291del
XM_017015582.1:c.248-9290_248-9288del	XP_016871071.1:n.248-9290_248-9288del
XM_017015583.1:c.248-9290_248-9288del	XP_016871072.1:n.248-9290_248-9288del
XM_024447781.1:c.-20-9293_-20-9291del	XP_024303549.1:n.-20-9293_-20-9291del
XR_001747009.2:n.1257-9290_1257-9288del
NM_001010848.4:c.1028-9290_1028-9288del MANE Select	NP_001010848.2:n.1028-9290_1028-9288del
NM_001370081.1:c.1028-9293_1028-9291del	NP_001357010.1:n.1028-9293_1028-9291del
NM_001370082.1:c.461-9290_461-9288del	NP_001357011.1:n.461-9290_461-9288del
NM_001370084.1:c.1028-9290_1028-9288del	NP_001357013.1:n.1028-9290_1028-9288del
NR_163251.1:n.1379-9293_1379-9291del
NR_163252.1:n.614-9293_614-9291del
NR_163253.1:n.1015-3013_1015-3011del
NM_001165973.2:c.365-9290_365-9288del	NP_001159445.1:n.365-9290_365-9288del