Canonical Allele Identifier: CA1538213631
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33955498C= , CM000667.2:g.33955498C= GRCh38
NC_000005.9:g.33955603C= , CM000667.1:g.33955603C= GRCh37
NC_000005.8:g.33991360C= NCBI36
NG_011691.2:g.34178G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296589.9:c.889-994G= MANE Select ENSP00000296589.4:n.889-994G=
ENST00000296589.8:c.889-994G= ENSP00000296589.4:n.889-994G=
ENST00000382102.7:c.889-994G= ENSP00000371534.3:n.889-994G=
ENST00000509381.1:c.563-994G= ENSP00000421100.1:n.563-994G=
ENST00000510600.1:c.364-994G= ENSP00000424010.1:n.364-994G=
NM_001012509.3:c.889-994G= NP_001012527.1:n.889-994G=
NM_001297417.2:c.563-994G= NP_001284346.2:n.563-994G=
NM_016180.4:c.889-994G= NP_057264.3:n.889-994G=
XM_011514051.1:c.487-994G= XP_011512353.1:n.487-994G=
XR_925620.1:n.1706-994G=
NM_016180.5:c.889-994G= MANE Select NP_057264.4:n.889-994G=
NM_001012509.4:c.889-994G= NP_001012527.2:n.889-994G=
NM_001297417.3:c.563-994G= NP_001284346.2:n.563-994G=
NM_001297417.4:c.563-994G= NP_001284346.2:n.563-994G=