Canonical Allele Identifier: CA791501291

Gene: AGA

Linked Data

• dbSNP Id: rs1289497134
• MyVariant Identifiers: chr4:g.178360386T>C (hg19) ; chr4:g.177439232T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439232T>C , CM000666.2:g.177439232T>C	GRCh38
NC_000004.11:g.178360386T>C , CM000666.1:g.178360386T>C	GRCh37
NC_000004.10:g.178597380T>C	NCBI36
NG_011845.2:g.8272A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.394+344A>G MANE Select	ENSP00000264595.2:n.394+344A>G
ENST00000264595.6:c.394+344A>G	ENSP00000264595.2:n.394+344A>G
ENST00000502310.5:c.49+344A>G	ENSP00000423798.1:n.49+344A>G
ENST00000506853.5:n.428+344A>G
ENST00000510635.1:c.90+344A>G
ENST00000510955.5:n.316-375A>G
NM_000027.3:c.394+344A>G	NP_000018.2:n.394+344A>G
NM_001171988.1:c.394+344A>G	NP_001165459.1:n.394+344A>G
NR_033655.1:n.522+344A>G
XM_006714123.2:c.394+344A>G	XP_006714186.1:n.394+344A>G
XR_001741155.2:n.488+344A>G
NM_000027.4:c.394+344A>G MANE Select	NP_000018.2:n.394+344A>G
NM_001171988.2:c.394+344A>G	NP_001165459.1:n.394+344A>G
NR_033655.2:n.456+344A>G