Canonical Allele Identifier: CA207963

Gene: GABRA1

Linked Data

• ClinVar Variation Id: 211057
• ClinVar RCV Id: RCV000194059
• dbSNP Id: rs797045590
• MyVariant Identifiers: chr5:g.161300309A>T (hg19) ; chr5:g.161873303A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161873303A>T , CM000667.2:g.161873303A>T	GRCh38
NC_000005.9:g.161300309A>T , CM000667.1:g.161300309A>T	GRCh37
NC_000005.8:g.161232887A>T	NCBI36
NG_011548.1:g.31113A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.442A>T MANE Select	ENSP00000377517.4:p.Ile148Phe
ENST00000635880.1:c.442A>T	ENSP00000489738.1:p.Ile148Phe
ENST00000635916.2:n.1217A>T
ENST00000636340.1:c.*291A>T	ENSP00000490002.1:n.*291A>T
ENST00000636408.1:n.246A>T
ENST00000636573.1:c.442A>T	ENSP00000490320.1:p.Ile148Phe
ENST00000637044.1:c.*216A>T	ENSP00000490684.1:n.*216A>T
ENST00000637827.1:c.442A>T	ENSP00000490804.1:p.Ile148Phe
ENST00000638112.1:c.442A>T	ENSP00000489839.1:p.Ile148Phe
ENST00000638159.1:c.487A>T	ENSP00000490360.1:p.Ile163Phe
ENST00000023897.10:c.442A>T	ENSP00000023897.6:p.Ile148Phe
ENST00000393943.9:c.442A>T	ENSP00000377517.4:p.Ile148Phe
ENST00000428797.7:c.442A>T	ENSP00000393097.2:p.Ile148Phe
ENST00000437025.6:c.442A>T	ENSP00000415441.2:p.Ile148Phe
ENST00000519542.1:n.206A>T
ENST00000519621.2:c.442A>T	ENSP00000430435.2:p.Ile148Phe
ENST00000634335.1:c.442A>T	ENSP00000489434.1:p.Ile148Phe
NM_000806.5:c.442A>T	NP_000797.2:p.Ile148Phe
NM_001127643.1:c.442A>T	NP_001121115.1:p.Ile148Phe
NM_001127644.1:c.442A>T	NP_001121116.1:p.Ile148Phe
NM_001127645.1:c.442A>T	NP_001121117.1:p.Ile148Phe
NM_001127648.1:c.442A>T	NP_001121120.1:p.Ile148Phe
NM_001127644.2:c.442A>T MANE Select	NP_001121116.1:p.Ile148Phe
NM_001127643.2:c.442A>T	NP_001121115.1:p.Ile148Phe
NM_001127645.2:c.442A>T	NP_001121117.1:p.Ile148Phe
NM_001127648.2:c.442A>T	NP_001121120.1:p.Ile148Phe