Canonical Allele Identifier: CA795448985

Gene: GABRA4

Linked Data

• dbSNP Id: rs1433334363
• gnomAD v3: 4-46927624-A-T
• gnomAD v4: 4-46927624-A-T
• MyVariant Identifiers: chr4:g.46929641A>T (hg19) ; chr4:g.46927624A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46927624A>T , CM000666.2:g.46927624A>T	GRCh38
NC_000004.11:g.46929641A>T , CM000666.1:g.46929641A>T	GRCh37
NC_000004.10:g.46624398A>T	NCBI36
NG_011809.1:g.70940T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.*601T>A MANE Select	ENSP00000264318.3:n.*601T>A
ENST00000264318.3:c.*601T>A	ENSP00000264318.3:n.*601T>A
NM_000809.3:c.*601T>A	NP_000800.2:n.*601T>A
NM_001204266.1:c.*601T>A	NP_001191195.1:n.*601T>A
NM_001204267.1:c.*601T>A	NP_001191196.1:n.*601T>A
XM_011513677.1:c.*601T>A	XP_011511979.1:n.*601T>A
NM_000809.4:c.*601T>A MANE Select	NP_000800.2:n.*601T>A
NM_001204266.2:c.*601T>A	NP_001191195.1:n.*601T>A
NM_001204267.2:c.*601T>A	NP_001191196.1:n.*601T>A