Canonical Allele Identifier: CA1866993798

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98541539_98541540delinsCT , CM000671.2:g.98541539_98541540delinsCT	GRCh38
NC_000009.11:g.101303821_101303822delinsCT , CM000671.1:g.101303821_101303822delinsCT	GRCh37
NC_000009.10:g.100343642_100343643delinsCT	NCBI36
NG_016426.1:g.172658_172659delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.630+333_630+334delinsAG MANE Select	ENSP00000259455.2:n.630+333_630+334delinsAG
ENST00000637410.1:n.408+333_408+334delinsAG
ENST00000259455.3:c.630+333_630+334delinsAG	ENSP00000259455.2:n.630+333_630+334delinsAG
ENST00000477471.1:n.417+333_417+334delinsAG
ENST00000634227.1:n.404+333_404+334delinsAG
NM_005458.7:c.630+333_630+334delinsAG	NP_005449.5:n.630+333_630+334delinsAG
XM_017015331.2:c.336+333_336+334delinsAG	XP_016870820.1:n.336+333_336+334delinsAG
NM_005458.8:c.630+333_630+334delinsAG MANE Select	NP_005449.5:n.630+333_630+334delinsAG