Canonical Allele Identifier: CA1538218683
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33984618C= , CM000667.2:g.33984618C= GRCh38
NC_000005.9:g.33984723C= , CM000667.1:g.33984723C= GRCh37
NC_000005.8:g.34020480C= NCBI36
NG_011691.2:g.5058G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.-35G= MANE Select ENSP00000296589.4:n.-35G=
ENST00000296589.8:c.-35G= ENSP00000296589.4:n.-35G=
ENST00000382102.7:c.-35G= ENSP00000371534.3:n.-35G=
ENST00000509381.1:c.-35G= ENSP00000421100.1:n.-35G=
NM_001012509.3:c.-35G= NP_001012527.1:n.-35G=
NM_001297417.2:c.-35G= NP_001284346.2:n.-35G=
NM_016180.4:c.-35G= NP_057264.3:n.-35G=
XM_011514052.1:c.-35G= XP_011512354.1:n.-35G=
XR_925620.1:n.527G=
NM_016180.5:c.-35G= MANE Select NP_057264.4:n.-35G=
NM_001012509.4:c.-35G= NP_001012527.2:n.-35G=
NM_001297417.3:c.-35G= NP_001284346.2:n.-35G=
NM_001297417.4:c.-35G= NP_001284346.2:n.-35G=