Canonical Allele Identifier: CA96639432

Gene: GABRA4

Linked Data

• dbSNP Id: rs1028307063
• gnomAD v3: 4-46927700-C-T
• gnomAD v4: 4-46927700-C-T
• MyVariant Identifiers: chr4:g.46929717C>T (hg19) ; chr4:g.46927700C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46927700C>T , CM000666.2:g.46927700C>T	GRCh38
NC_000004.11:g.46929717C>T , CM000666.1:g.46929717C>T	GRCh37
NC_000004.10:g.46624474C>T	NCBI36
NG_011809.1:g.70864G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.*525G>A MANE Select	ENSP00000264318.3:n.*525G>A
ENST00000264318.3:c.*525G>A	ENSP00000264318.3:n.*525G>A
NM_000809.3:c.*525G>A	NP_000800.2:n.*525G>A
NM_001204266.1:c.*525G>A	NP_001191195.1:n.*525G>A
NM_001204267.1:c.*525G>A	NP_001191196.1:n.*525G>A
XM_011513677.1:c.*525G>A	XP_011511979.1:n.*525G>A
NM_000809.4:c.*525G>A MANE Select	NP_000800.2:n.*525G>A
NM_001204266.2:c.*525G>A	NP_001191195.1:n.*525G>A
NM_001204267.2:c.*525G>A	NP_001191196.1:n.*525G>A