Canonical Allele Identifier: CA2765834830
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951746del , CM000667.2:g.33951746del GRCh38
NC_000005.9:g.33951851del , CM000667.1:g.33951851del GRCh37
NC_000005.8:g.33987608del NCBI36
NG_011691.2:g.37930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1033-69del MANE Select ENSP00000296589.4:n.1033-69del
ENST00000296589.8:c.1033-69del ENSP00000296589.4:n.1033-69del
ENST00000382102.7:c.1033-69del ENSP00000371534.3:n.1033-69del
ENST00000509381.1:c.707-69del ENSP00000421100.1:n.707-69del
ENST00000510600.1:c.508-69del ENSP00000424010.1:n.508-69del
NM_001012509.3:c.1033-69del NP_001012527.1:n.1033-69del
NM_001297417.2:c.707-69del NP_001284346.2:n.707-69del
NM_016180.4:c.1033-69del NP_057264.3:n.1033-69del
XM_011514051.1:c.631-69del XP_011512353.1:n.631-69del
XR_925620.1:n.1850-69del
NM_016180.5:c.1033-69del MANE Select NP_057264.4:n.1033-69del
NM_001012509.4:c.1033-69del NP_001012527.2:n.1033-69del
NM_001297417.3:c.707-69del NP_001284346.2:n.707-69del
NM_001297417.4:c.707-69del NP_001284346.2:n.707-69del