Canonical Allele Identifier: CA1538195691
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33963676A= , CM000667.2:g.33963676A= GRCh38
NC_000005.9:g.33963781A= , CM000667.1:g.33963781A= GRCh37
NC_000005.8:g.33999538A= NCBI36
NG_011691.2:g.26000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296589.9:c.888+15T= MANE Select ENSP00000296589.4:n.888+15T=
ENST00000296589.8:c.888+15T= ENSP00000296589.4:n.888+15T=
ENST00000382102.7:c.888+15T= ENSP00000371534.3:n.888+15T=
ENST00000505056.1:n.705T=
ENST00000509381.1:c.563-9172T= ENSP00000421100.1:n.563-9172T=
ENST00000510600.1:c.363+15T= ENSP00000424010.1:n.363+15T=
NM_001012509.3:c.888+15T= NP_001012527.1:n.888+15T=
NM_001297417.2:c.563-9172T= NP_001284346.2:n.563-9172T=
NM_016180.4:c.888+15T= NP_057264.3:n.888+15T=
XM_011514051.1:c.486+15T= XP_011512353.1:n.486+15T=
XM_011514052.1:c.888+15T= XP_011512354.1:n.888+15T=
XR_925620.1:n.1705+15T=
NM_016180.5:c.888+15T= MANE Select NP_057264.4:n.888+15T=
NM_001012509.4:c.888+15T= NP_001012527.2:n.888+15T=
NM_001297417.3:c.563-9172T= NP_001284346.2:n.563-9172T=
NM_001297417.4:c.563-9172T= NP_001284346.2:n.563-9172T=