Canonical Allele Identifier: CA96639357

Gene: GABRA4

Linked Data

• dbSNP Id: rs1056831470
• MyVariant Identifiers: chr4:g.46929528T>A (hg19) ; chr4:g.46927511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46927511T>A , CM000666.2:g.46927511T>A	GRCh38
NC_000004.11:g.46929528T>A , CM000666.1:g.46929528T>A	GRCh37
NC_000004.10:g.46624285T>A	NCBI36
NG_011809.1:g.71053A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264318.4:c.*714A>T MANE Select	ENSP00000264318.3:n.*714A>T
ENST00000264318.3:c.*714A>T	ENSP00000264318.3:n.*714A>T
NM_000809.3:c.*714A>T	NP_000800.2:n.*714A>T
NM_001204266.1:c.*714A>T	NP_001191195.1:n.*714A>T
NM_001204267.1:c.*714A>T	NP_001191196.1:n.*714A>T
XM_011513677.1:c.*714A>T	XP_011511979.1:n.*714A>T
NM_000809.4:c.*714A>T MANE Select	NP_000800.2:n.*714A>T
NM_001204266.2:c.*714A>T	NP_001191195.1:n.*714A>T
NM_001204267.2:c.*714A>T	NP_001191196.1:n.*714A>T