Canonical Allele Identifier: CA356778026

Gene: GABRA4

Linked Data

• MyVariant Identifiers: chr4:g.46995427C>G (hg19) ; chr4:g.46993410C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993410C>G , CM000666.2:g.46993410C>G	GRCh38
NC_000004.11:g.46995427C>G , CM000666.1:g.46995427C>G	GRCh37
NC_000004.10:g.46690184C>G	NCBI36
NG_011809.1:g.5154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.15G>C MANE Select	ENSP00000264318.3:p.Lys5Asn
ENST00000264318.3:c.15G>C	ENSP00000264318.3:p.Lys5Asn
ENST00000502874.1:c.15G>C	ENSP00000424386.1:p.Lys5Asn
ENST00000508560.5:c.15G>C	ENSP00000425445.1:p.Lys5Asn
ENST00000509316.1:n.139G>C
ENST00000511523.5:c.15G>C	ENSP00000422152.1:p.Lys5Asn
NM_000809.3:c.15G>C	NP_000800.2:p.Lys5Asn
NM_001204266.1:c.26G>C	NP_001191195.1:p.Arg9Thr
NM_001204267.1:c.26G>C	NP_001191196.1:p.Arg9Thr
XM_011513677.1:c.15G>C	XP_011511979.1:p.Lys5Asn
NM_000809.4:c.15G>C MANE Select	NP_000800.2:p.Lys5Asn
NM_001204266.2:c.26G>C	NP_001191195.1:p.Arg9Thr
NM_001204267.2:c.26G>C	NP_001191196.1:p.Arg9Thr