Canonical Allele Identifier: CA1515637344
Gene: AGA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434320T= , CM000666.2:g.177434320T= GRCh38
NC_000004.11:g.178355474T= , CM000666.1:g.178355474T= GRCh37
NC_000004.10:g.178592468T= NCBI36
NG_011845.2:g.13184A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264595.7:c.806+62A= MANE Select ENSP00000264595.2:n.806+62A=
ENST00000264595.6:c.806+62A= ENSP00000264595.2:n.806+62A=
ENST00000502310.5:c.377+62A= ENSP00000423798.1:n.377+62A=
NM_000027.3:c.806+62A= NP_000018.2:n.806+62A=
NM_001171988.1:c.776+62A= NP_001165459.1:n.776+62A=
NR_033655.1:n.858+62A=
XR_001741155.2:n.878+62A=
NM_000027.4:c.806+62A= MANE Select NP_000018.2:n.806+62A=
NM_001171988.2:c.776+62A= NP_001165459.1:n.776+62A=
NR_033655.2:n.792+62A=
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