Canonical Allele Identifier: CA2907362

Gene: GABRA4

Linked Data

• dbSNP Id: rs766116799
• ExAC: 4:46995466 C / A
• gnomAD v2: 4-46995466-C-A
• gnomAD v4: 4-46993449-C-A
• MyVariant Identifiers: chr4:g.46995466C>A (hg19) ; chr4:g.46993449C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993449C>A , CM000666.2:g.46993449C>A	GRCh38
NC_000004.11:g.46995466C>A , CM000666.1:g.46995466C>A	GRCh37
NC_000004.10:g.46690223C>A	NCBI36
NG_011809.1:g.5115G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.-25G>T MANE Select	ENSP00000264318.3:n.-25G>T
ENST00000264318.3:c.-25G>T	ENSP00000264318.3:n.-25G>T
ENST00000502874.1:c.-25G>T	ENSP00000424386.1:n.-25G>T
ENST00000508560.5:c.-25G>T	ENSP00000425445.1:n.-25G>T
ENST00000509316.1:n.100G>T
ENST00000511523.5:c.-25G>T	ENSP00000422152.1:n.-25G>T
NM_000809.3:c.-25G>T	NP_000800.2:n.-25G>T
NM_001204266.1:c.-14G>T	NP_001191195.1:n.-14G>T
NM_001204267.1:c.-14G>T	NP_001191196.1:n.-14G>T
XM_011513677.1:c.-25G>T	XP_011511979.1:n.-25G>T
NM_000809.4:c.-25G>T MANE Select	NP_000800.2:n.-25G>T
NM_001204266.2:c.-14G>T	NP_001191195.1:n.-14G>T
NM_001204267.2:c.-14G>T	NP_001191196.1:n.-14G>T