Canonical Allele Identifier: CA2672747662

Gene: AGA

Linked Data

• gnomAD v4: 4-177438910-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438910C>T , CM000666.2:g.177438910C>T	GRCh38
NC_000004.11:g.178360064C>T , CM000666.1:g.178360064C>T	GRCh37
NC_000004.10:g.178597058C>T	NCBI36
NG_011845.2:g.8594G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.395-53G>A MANE Select	ENSP00000264595.2:n.395-53G>A
ENST00000264595.6:c.395-53G>A	ENSP00000264595.2:n.395-53G>A
ENST00000502310.5:c.50-53G>A	ENSP00000423798.1:n.50-53G>A
ENST00000506853.5:n.429-53G>A
ENST00000510635.1:c.91-53G>A
ENST00000510955.5:n.316-53G>A
NM_000027.3:c.395-53G>A	NP_000018.2:n.395-53G>A
NM_001171988.1:c.395-53G>A	NP_001165459.1:n.395-53G>A
NR_033655.1:n.523-53G>A
XM_006714123.2:c.395-53G>A	XP_006714186.1:n.395-53G>A
XR_001741155.2:n.489-53G>A
NM_000027.4:c.395-53G>A MANE Select	NP_000018.2:n.395-53G>A
NM_001171988.2:c.395-53G>A	NP_001165459.1:n.395-53G>A
NR_033655.2:n.457-53G>A