Canonical Allele Identifier: CA556484221

Gene: AGA

Linked Data

• gnomAD v2: 4-178360322-G-A
• gnomAD v3: 4-177439168-G-A
• gnomAD v4: 4-177439168-G-A
• MyVariant Identifiers: chr4:g.178360322G>A (hg19) ; chr4:g.177439168G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439168G>A , CM000666.2:g.177439168G>A	GRCh38
NC_000004.11:g.178360322G>A , CM000666.1:g.178360322G>A	GRCh37
NC_000004.10:g.178597316G>A	NCBI36
NG_011845.2:g.8336C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.395-311C>T MANE Select	ENSP00000264595.2:n.395-311C>T
ENST00000264595.6:c.395-311C>T	ENSP00000264595.2:n.395-311C>T
ENST00000502310.5:c.50-311C>T	ENSP00000423798.1:n.50-311C>T
ENST00000506853.5:n.429-311C>T
ENST00000510635.1:c.91-311C>T
ENST00000510955.5:n.316-311C>T
NM_000027.3:c.395-311C>T	NP_000018.2:n.395-311C>T
NM_001171988.1:c.395-311C>T	NP_001165459.1:n.395-311C>T
NR_033655.1:n.523-311C>T
XM_006714123.2:c.395-311C>T	XP_006714186.1:n.395-311C>T
XR_001741155.2:n.489-311C>T
NM_000027.4:c.395-311C>T MANE Select	NP_000018.2:n.395-311C>T
NM_001171988.2:c.395-311C>T	NP_001165459.1:n.395-311C>T
NR_033655.2:n.457-311C>T