Canonical Allele Identifier: CA1557615409
Gene: ARSB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.78780465_78780466delinsCG , CM000667.2:g.78780465_78780466delinsCG GRCh38
NC_000005.9:g.78076288_78076289delinsCG , CM000667.1:g.78076288_78076289delinsCG GRCh37
NC_000005.8:g.78112044_78112045delinsCG NCBI36
NG_007089.1:g.211069_211070delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264914.10:c.1533_1534delinsCG MANE Select ENSP00000264914.4:p.Pro511=
ENST00000264914.8:c.1533_1534delinsCG ENSP00000264914.4:p.Pro511=
ENST00000521011.1:n.498_499delinsCG
NM_000046.3:c.1533_1534delinsCG NP_000037.2:p.Pro511=
XM_011543390.1:c.1533_1534delinsCG XP_011541692.1:p.Pro511=
NM_000046.4:c.1533_1534delinsCG NP_000037.2:p.Pro511=
NM_000046.5:c.1533_1534delinsCG MANE Select NP_000037.2:p.Pro511=
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