Canonical Allele Identifier: CA1515649858
Gene: AGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177442426C= , CM000666.2:g.177442426C= GRCh38
NC_000004.11:g.178363580C= , CM000666.1:g.178363580C= GRCh37
NC_000004.10:g.178600574C= NCBI36
NG_011845.2:g.5078G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.-51G= MANE Select ENSP00000264595.2:n.-51G=
ENST00000264595.6:c.-51G= ENSP00000264595.2:n.-51G=
NM_000027.3:c.-51G= NP_000018.2:n.-51G=
NM_001171988.1:c.-51G= NP_001165459.1:n.-51G=
NR_033655.1:n.78G=
XM_006714123.2:c.-51G= XP_006714186.1:n.-51G=
XR_001741155.2:n.44G=
NM_000027.4:c.-51G= MANE Select NP_000018.2:n.-51G=
NM_001171988.2:c.-51G= NP_001165459.1:n.-51G=
NR_033655.2:n.12G=