Canonical Allele Identifier: CA930509955

Gene: NRG3

Linked Data

• dbSNP Id: rs2064007557
• gnomAD v3: 10-82059281-TGGGC-T
• gnomAD v4: 10-82059281-TGGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.82059282_82059285del , CM000672.2:g.82059282_82059285del	GRCh38
NC_000010.10:g.83819038_83819041del , CM000672.1:g.83819038_83819041del	GRCh37
NC_000010.9:g.83809018_83809021del	NCBI36
NG_013373.1:g.188969_188972del

Transcript Alleles

HGVS	Amino-acid change
ENST00000372141.7:c.823+183119_823+183122del MANE Select	ENSP00000361214.2:n.823+183119_823+183122...
ENST00000372141.6:c.823+183119_823+183122del	ENSP00000361214.2:n.823+183119_823+183122...
ENST00000372142.6:c.61-107445_61-107442del	ENSP00000361215.2:n.61-107445_61-107442de...
ENST00000404547.5:c.823+183119_823+183122del	ENSP00000384796.1:n.823+183119_823+183122...
ENST00000404576.6:c.136-107445_136-107442del	ENSP00000385804.2:n.136-107445_136-107442...
ENST00000555784.5:c.135+181187_135+181190del	ENSP00000451858.1:n.135+181187_135+181190...
ENST00000556918.5:c.136-107445_136-107442del	ENSP00000451376.1:n.136-107445_136-107442...
ENST00000602794.5:c.*371+169617_*371+169620del	ENSP00000473669.1:n.*371+169617_*371+1696...
NM_001010848.3:c.823+183119_823+183122del	NP_001010848.2:n.823+183119_823+183122del...
NM_001165972.1:c.823+183119_823+183122del	NP_001159444.1:n.823+183119_823+183122del...
NM_001165973.1:c.61-107445_61-107442del	NP_001159445.1:n.61-107445_61-107442del
XM_005269444.3:c.823+183119_823+183122del	XP_005269501.1:n.823+183119_823+183122del...
XM_011539172.1:c.823+183119_823+183122del	XP_011537474.1:n.823+183119_823+183122del...
XM_011539173.1:c.823+183119_823+183122del	XP_011537475.1:n.823+183119_823+183122del...
XM_011539174.1:c.823+183119_823+183122del	XP_011537476.1:n.823+183119_823+183122del...
XM_011539175.1:c.823+183119_823+183122del	XP_011537477.1:n.823+183119_823+183122del...
XM_005269444.5:c.823+183119_823+183122del	XP_005269501.1:n.823+183119_823+183122del...
XM_011539172.3:c.823+183119_823+183122del	XP_011537474.1:n.823+183119_823+183122del...
XM_011539173.3:c.823+183119_823+183122del	XP_011537475.1:n.823+183119_823+183122del...
XM_011539175.3:c.823+183119_823+183122del	XP_011537477.1:n.823+183119_823+183122del...
XM_017015573.2:c.824-173460_824-173457del	XP_016871062.1:n.824-173460_824-173457del...
XM_017015574.2:c.824-173460_824-173457del	XP_016871063.1:n.824-173460_824-173457del...
XM_017015575.2:c.824-173460_824-173457del	XP_016871064.1:n.824-173460_824-173457del...
XM_017015576.2:c.824-173460_824-173457del	XP_016871065.1:n.824-173460_824-173457del...
XM_017015577.2:c.824-173460_824-173457del	XP_016871066.1:n.824-173460_824-173457del...
XM_017015578.2:c.824-173460_824-173457del	XP_016871067.1:n.824-173460_824-173457del...
XM_017015579.2:c.824-173460_824-173457del	XP_016871068.1:n.824-173460_824-173457del...
XM_017015580.2:c.824-173460_824-173457del	XP_016871069.1:n.824-173460_824-173457del...
XM_017015581.2:c.823+183119_823+183122del	XP_016871070.1:n.823+183119_823+183122del...
XM_017015584.2:c.824-173460_824-173457del	XP_016871073.1:n.824-173460_824-173457del...
XR_001747009.2:n.975-173460_975-173457del
NM_001010848.4:c.823+183119_823+183122del MANE Select	NP_001010848.2:n.823+183119_823+183122del...
NM_001370081.1:c.823+183119_823+183122del	NP_001357010.1:n.823+183119_823+183122del...
NM_001370082.1:c.79-107445_79-107442del	NP_001357011.1:n.79-107445_79-107442del
NM_001370083.1:c.823+183119_823+183122del	NP_001357012.1:n.823+183119_823+183122del...
NM_001370084.1:c.823+183119_823+183122del	NP_001357013.1:n.823+183119_823+183122del...
NR_163251.1:n.971-92121_971-92118del
NR_163252.1:n.409+181187_409+181190del
NR_163253.1:n.810+169617_810+169620del
NM_001165973.2:c.61-107445_61-107442del	NP_001159445.1:n.61-107445_61-107442del