Canonical Allele Identifier: CA1515637815
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434507C= , CM000666.2:g.177434507C= GRCh38
NC_000004.11:g.178355661C= , CM000666.1:g.178355661C= GRCh37
NC_000004.10:g.178592655C= NCBI36
NG_011845.2:g.12997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.699-18G= MANE Select ENSP00000264595.2:n.699-18G=
ENST00000264595.6:c.699-18G= ENSP00000264595.2:n.699-18G=
ENST00000502310.5:c.278-26G= ENSP00000423798.1:n.278-26G=
ENST00000506853.5:n.657-18G=
ENST00000510635.1:c.373-26G=
NM_000027.3:c.699-18G= NP_000018.2:n.699-18G=
NM_001171988.1:c.677-26G= NP_001165459.1:n.677-26G=
NR_033655.1:n.751-18G=
XM_006714123.2:c.677-18G= XP_006714186.1:n.677-18G=
XR_001741155.2:n.771-18G=
NM_000027.4:c.699-18G= MANE Select NP_000018.2:n.699-18G=
NM_001171988.2:c.677-26G= NP_001165459.1:n.677-26G=
NR_033655.2:n.685-18G=