Canonical Allele Identifier: CA1538218477
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33984249A= , CM000667.2:g.33984249A= GRCh38
NC_000005.9:g.33984354A= , CM000667.1:g.33984354A= GRCh37
NC_000005.8:g.34020111A= NCBI36
NG_011691.2:g.5427T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.335T= MANE Select ENSP00000296589.4:p.Met112=
ENST00000296589.8:c.335T= ENSP00000296589.4:p.Met112=
ENST00000382102.7:c.335T= ENSP00000371534.3:p.Met112=
ENST00000505056.1:n.314T=
ENST00000509381.1:c.335T= ENSP00000421100.1:p.Met112=
NM_001012509.3:c.335T= NP_001012527.1:p.Met112=
NM_001297417.2:c.335T= NP_001284346.2:p.Met112=
NM_016180.4:c.335T= NP_057264.3:p.Met112=
XM_011514052.1:c.335T= XP_011512354.1:p.Met112=
XR_925620.1:n.896T=
NM_016180.5:c.335T= MANE Select NP_057264.4:p.Met112=
NM_001012509.4:c.335T= NP_001012527.2:p.Met112=
NM_001297417.3:c.335T= NP_001284346.2:p.Met112=
NM_001297417.4:c.335T= NP_001284346.2:p.Met112=