Canonical Allele Identifier: CA96628008

Gene: GABRA4

Linked Data

• dbSNP Id: rs113770312
• MyVariant Identifiers: chr4:g.46973443G>T (hg19) ; chr4:g.46971426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.46971426G>T , CM000666.2:g.46971426G>T	GRCh38
NC_000004.11:g.46973443G>T , CM000666.1:g.46973443G>T	GRCh37
NC_000004.10:g.46668200G>T	NCBI36
NG_011809.1:g.27138C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264318.4:c.722-191C>A MANE Select	ENSP00000264318.3:n.722-191C>A
ENST00000264318.3:c.722-191C>A	ENSP00000264318.3:n.722-191C>A
ENST00000502874.1:c.*492-191C>A	ENSP00000424386.1:n.*492-191C>A
ENST00000508560.5:c.*543-191C>A	ENSP00000425445.1:n.*543-191C>A
ENST00000511523.5:c.*542+2806C>A	ENSP00000422152.1:n.*542+2806C>A
NM_000809.3:c.722-191C>A	NP_000800.2:n.722-191C>A
NM_001204266.1:c.665-191C>A	NP_001191195.1:n.665-191C>A
NM_001204267.1:c.664+2806C>A	NP_001191196.1:n.664+2806C>A
XM_011513677.1:c.721+2806C>A	XP_011511979.1:n.721+2806C>A
NM_000809.4:c.722-191C>A MANE Select	NP_000800.2:n.722-191C>A
NM_001204266.2:c.665-191C>A	NP_001191195.1:n.665-191C>A
NM_001204267.2:c.664+2806C>A	NP_001191196.1:n.664+2806C>A