Canonical Allele Identifier: CA356778029

Gene: GABRA4

Linked Data

• MyVariant Identifiers: chr4:g.46995428T>A (hg19) ; chr4:g.46993411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46993411T>A , CM000666.2:g.46993411T>A	GRCh38
NC_000004.11:g.46995428T>A , CM000666.1:g.46995428T>A	GRCh37
NC_000004.10:g.46690185T>A	NCBI36
NG_011809.1:g.5153A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.14A>T MANE Select	ENSP00000264318.3:p.Lys5Met
ENST00000264318.3:c.14A>T	ENSP00000264318.3:p.Lys5Met
ENST00000502874.1:c.14A>T	ENSP00000424386.1:p.Lys5Met
ENST00000508560.5:c.14A>T	ENSP00000425445.1:p.Lys5Met
ENST00000509316.1:n.138A>T
ENST00000511523.5:c.14A>T	ENSP00000422152.1:p.Lys5Met
NM_000809.3:c.14A>T	NP_000800.2:p.Lys5Met
NM_001204266.1:c.25A>T	NP_001191195.1:p.Arg9Ter
NM_001204267.1:c.25A>T	NP_001191196.1:p.Arg9Ter
XM_011513677.1:c.14A>T	XP_011511979.1:p.Lys5Met
NM_000809.4:c.14A>T MANE Select	NP_000800.2:p.Lys5Met
NM_001204266.2:c.25A>T	NP_001191195.1:p.Arg9Ter
NM_001204267.2:c.25A>T	NP_001191196.1:p.Arg9Ter