Canonical Allele Identifier: CA2676320917

Gene: GABRA1

Linked Data

• gnomAD v4: 5-161848291-C-CTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161848291_161848292insTCG , CM000667.2:g.161848291_161848292insTCG	GRCh38
NC_000005.9:g.161275297_161275298insTCG , CM000667.1:g.161275297_161275298insTCG	GRCh37
NC_000005.8:g.161207875_161207876insTCG	NCBI36
NG_011548.1:g.6101_6102insTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.-147_-146insTCG MANE Select	ENSP00000377517.4:n.-147_-146insTCG
ENST00000635916.2:n.629_630insTCG
ENST00000637044.1:c.-147_-146insTCG	ENSP00000490684.1:n.-147_-146insTCG
ENST00000638112.1:c.-147_-146insTCG	ENSP00000489839.1:n.-147_-146insTCG
ENST00000023897.10:c.-147_-146insTCG	ENSP00000023897.6:n.-147_-146insTCG
ENST00000393943.9:c.-147_-146insTCG	ENSP00000377517.4:n.-147_-146insTCG
ENST00000428797.7:c.-147_-146insTCG	ENSP00000393097.2:n.-147_-146insTCG
ENST00000635096.1:c.-147_-146insTCG	ENSP00000489033.1:n.-147_-146insTCG
NM_000806.5:c.-147_-146insTCG	NP_000797.2:n.-147_-146insTCG
NM_001127643.1:c.-147_-146insTCG	NP_001121115.1:n.-147_-146insTCG
NM_001127644.1:c.-147_-146insTCG	NP_001121116.1:n.-147_-146insTCG
XR_941158.3:n.89+2228_89+2229insCGA
NM_001127644.2:c.-147_-146insTCG MANE Select	NP_001121116.1:n.-147_-146insTCG
NM_001127643.2:c.-147_-146insTCG	NP_001121115.1:n.-147_-146insTCG