Canonical Allele Identifier: CA442332817

Gene: AGA

Linked Data

• dbSNP Id: rs1162483846
• gnomAD v2: 4-178360782-C-T
• gnomAD v4: 4-177439628-C-T
• MyVariant Identifiers: chr4:g.178360782C>T (hg19) ; chr4:g.177439628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439628C>T , CM000666.2:g.177439628C>T	GRCh38
NC_000004.11:g.178360782C>T , CM000666.1:g.178360782C>T	GRCh37
NC_000004.10:g.178597776C>T	NCBI36
NG_011845.2:g.7876G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.342G>A MANE Select	ENSP00000264595.2:p.Val114=
ENST00000264595.6:c.342G>A	ENSP00000264595.2:p.Val114=
ENST00000506853.5:n.376G>A
ENST00000510635.1:c.38G>A
ENST00000510955.5:n.315+645G>A
NM_000027.3:c.342G>A	NP_000018.2:p.Val114=
NM_001171988.1:c.342G>A	NP_001165459.1:p.Val114=
NR_033655.1:n.470G>A
XM_006714123.2:c.342G>A	XP_006714186.1:p.Val114=
XR_001741155.2:n.436G>A
NM_000027.4:c.342G>A MANE Select	NP_000018.2:p.Val114=
NM_001171988.2:c.342G>A	NP_001165459.1:p.Val114=
NR_033655.2:n.404G>A