Canonical Allele Identifier: CA2676323768

Gene: GABRA1

Linked Data

• gnomAD v4: 5-161897903-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161897903T>C , CM000667.2:g.161897903T>C	GRCh38
NC_000005.9:g.161324909T>C , CM000667.1:g.161324909T>C	GRCh37
NC_000005.8:g.161257487T>C	NCBI36
NG_011548.1:g.55713T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000393943.10:c.*481T>C MANE Select	ENSP00000377517.4:n.*481T>C
ENST00000635916.2:n.4695T>C
ENST00000636340.1:c.*1701T>C	ENSP00000490002.1:n.*1701T>C
ENST00000636408.1:n.1656T>C
ENST00000636573.1:c.*481T>C	ENSP00000490320.1:n.*481T>C
ENST00000637044.1:c.*1626T>C	ENSP00000490684.1:n.*1626T>C
ENST00000638112.1:c.*481T>C	ENSP00000489839.1:n.*481T>C
ENST00000638159.1:c.*481T>C	ENSP00000490360.1:n.*481T>C
ENST00000393943.9:c.*481T>C	ENSP00000377517.4:n.*481T>C
ENST00000428797.7:c.*481T>C	ENSP00000393097.2:n.*481T>C
ENST00000437025.6:c.*481T>C	ENSP00000415441.2:n.*481T>C
NM_000806.5:c.*481T>C	NP_000797.2:n.*481T>C
NM_001127643.1:c.*481T>C	NP_001121115.1:n.*481T>C
NM_001127644.1:c.*481T>C	NP_001121116.1:n.*481T>C
NM_001127645.1:c.*481T>C	NP_001121117.1:n.*481T>C
NM_001127648.1:c.*481T>C	NP_001121120.1:n.*481T>C
NM_001127644.2:c.*481T>C MANE Select	NP_001121116.1:n.*481T>C
NM_001127643.2:c.*481T>C	NP_001121115.1:n.*481T>C
NM_001127645.2:c.*481T>C	NP_001121117.1:n.*481T>C
NM_001127648.2:c.*481T>C	NP_001121120.1:n.*481T>C