Canonical Allele Identifier: CA1596250028

Gene: GABRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161848240_161848241delinsAG , CM000667.2:g.161848240_161848241delinsAG	GRCh38
NC_000005.9:g.161275246_161275247delinsAG , CM000667.1:g.161275246_161275247delinsAG	GRCh37
NC_000005.8:g.161207824_161207825delinsAG	NCBI36
NG_011548.1:g.6050_6051delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.-198_-197delinsAG MANE Select	ENSP00000377517.4:n.-198_-197delinsAG
ENST00000635916.2:n.578_579delinsAG
ENST00000638112.1:c.-198_-197delinsAG	ENSP00000489839.1:n.-198_-197delinsAG
ENST00000023897.10:c.-198_-197delinsAG	ENSP00000023897.6:n.-198_-197delinsAG
ENST00000393943.9:c.-198_-197delinsAG	ENSP00000377517.4:n.-198_-197delinsAG
ENST00000428797.7:c.-198_-197delinsAG	ENSP00000393097.2:n.-198_-197delinsAG
ENST00000635096.1:c.-198_-197delinsAG	ENSP00000489033.1:n.-198_-197delinsAG
NM_000806.5:c.-198_-197delinsAG	NP_000797.2:n.-198_-197delinsAG
NM_001127643.1:c.-198_-197delinsAG	NP_001121115.1:n.-198_-197delinsAG
NM_001127644.1:c.-198_-197delinsAG	NP_001121116.1:n.-198_-197delinsAG
XR_941158.3:n.89+2279_89+2280delinsCT
NM_001127644.2:c.-198_-197delinsAG MANE Select	NP_001121116.1:n.-198_-197delinsAG
NM_001127643.2:c.-198_-197delinsAG	NP_001121115.1:n.-198_-197delinsAG