Canonical Allele Identifier: CA131087778

Gene: GABRA1

Linked Data

• dbSNP Id: rs527416473
• gnomAD v3: 5-161895785-T-C
• gnomAD v4: 5-161895785-T-C
• MyVariant Identifiers: chr5:g.161322791T>C (hg19) ; chr5:g.161895785T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161895785T>C , CM000667.2:g.161895785T>C	GRCh38
NC_000005.9:g.161322791T>C , CM000667.1:g.161322791T>C	GRCh37
NC_000005.8:g.161255369T>C	NCBI36
NG_011548.1:g.53595T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393943.10:c.976T>C MANE Select	ENSP00000377517.4:p.Ser326Pro
ENST00000635880.1:c.976T>C	ENSP00000489738.1:p.Ser326Pro
ENST00000635916.2:n.2577T>C
ENST00000636340.1:c.*825T>C	ENSP00000490002.1:n.*825T>C
ENST00000636408.1:n.780T>C
ENST00000636573.1:c.976T>C	ENSP00000490320.1:p.Ser326Pro
ENST00000637044.1:c.*750T>C	ENSP00000490684.1:n.*750T>C
ENST00000637827.1:c.976T>C	ENSP00000490804.1:p.Ser326Pro
ENST00000638112.1:c.976T>C	ENSP00000489839.1:p.Ser326Pro
ENST00000638159.1:c.1021T>C	ENSP00000490360.1:p.Ser341Pro
ENST00000023897.10:c.976T>C	ENSP00000023897.6:p.Ser326Pro
ENST00000393943.9:c.976T>C	ENSP00000377517.4:p.Ser326Pro
ENST00000428797.7:c.976T>C	ENSP00000393097.2:p.Ser326Pro
ENST00000437025.6:c.976T>C	ENSP00000415441.2:p.Ser326Pro
NM_000806.5:c.976T>C	NP_000797.2:p.Ser326Pro
NM_001127643.1:c.976T>C	NP_001121115.1:p.Ser326Pro
NM_001127644.1:c.976T>C	NP_001121116.1:p.Ser326Pro
NM_001127645.1:c.976T>C	NP_001121117.1:p.Ser326Pro
NM_001127648.1:c.976T>C	NP_001121120.1:p.Ser326Pro
NM_001127644.2:c.976T>C MANE Select	NP_001121116.1:p.Ser326Pro
NM_001127643.2:c.976T>C	NP_001121115.1:p.Ser326Pro
NM_001127645.2:c.976T>C	NP_001121117.1:p.Ser326Pro
NM_001127648.2:c.976T>C	NP_001121120.1:p.Ser326Pro