Canonical Allele Identifier: CA131081745

Gene: GABRA1

Linked Data

• dbSNP Id: rs531965222
• gnomAD v3: 5-161848270-C-T
• gnomAD v4: 5-161848270-C-T
• MyVariant Identifiers: chr5:g.161275276C>T (hg19) ; chr5:g.161848270C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.161848270C>T , CM000667.2:g.161848270C>T	GRCh38
NC_000005.9:g.161275276C>T , CM000667.1:g.161275276C>T	GRCh37
NC_000005.8:g.161207854C>T	NCBI36
NG_011548.1:g.6080C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393943.10:c.-168C>T MANE Select	ENSP00000377517.4:n.-168C>T
ENST00000635916.2:n.608C>T
ENST00000637044.1:c.-168C>T	ENSP00000490684.1:n.-168C>T
ENST00000638112.1:c.-168C>T	ENSP00000489839.1:n.-168C>T
ENST00000023897.10:c.-168C>T	ENSP00000023897.6:n.-168C>T
ENST00000393943.9:c.-168C>T	ENSP00000377517.4:n.-168C>T
ENST00000428797.7:c.-168C>T	ENSP00000393097.2:n.-168C>T
ENST00000635096.1:c.-168C>T	ENSP00000489033.1:n.-168C>T
NM_000806.5:c.-168C>T	NP_000797.2:n.-168C>T
NM_001127643.1:c.-168C>T	NP_001121115.1:n.-168C>T
NM_001127644.1:c.-168C>T	NP_001121116.1:n.-168C>T
XR_941158.3:n.89+2250G>A
NM_001127644.2:c.-168C>T MANE Select	NP_001121116.1:n.-168C>T
NM_001127643.2:c.-168C>T	NP_001121115.1:n.-168C>T