Canonical Allele Identifier: CA1955682543
Gene: SPTY2D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18611484C= , CM000673.2:g.18611484C= GRCh38
NC_000011.9:g.18633031C= , CM000673.1:g.18633031C= GRCh37
NC_000011.8:g.18589607C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336349.6:c.1957G= MANE Select ENSP00000337991.5:p.Ala653=
ENST00000336349.5:c.1957G= ENSP00000337991.5:p.Ala653=
NM_194285.2:c.1957G= NP_919261.2:p.Ala653=
XM_011519919.1:c.1705G= XP_011518221.1:p.Ala569=
XM_011519919.2:c.1705G= XP_011518221.1:p.Ala569=
NM_194285.3:c.1957G= MANE Select NP_919261.2:p.Ala653=