Canonical Allele Identifier: CA1538206728
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33944787A= , CM000667.2:g.33944787A= GRCh38
NC_000005.9:g.33944892A= , CM000667.1:g.33944892A= GRCh37
NC_000005.8:g.33980649A= NCBI36
NG_011691.2:g.44889T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1454T= MANE Select ENSP00000296589.4:p.Leu485=
ENST00000296589.8:c.1454T= ENSP00000296589.4:p.Leu485=
NM_016180.4:c.1454T= NP_057264.3:p.Leu485=
XM_011514051.1:c.1052T= XP_011512353.1:p.Leu351=
NM_016180.5:c.1454T= MANE Select NP_057264.4:p.Leu485=