Canonical Allele Identifier: CA2673476835
Gene: SLC45A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951327del , CM000667.2:g.33951327del GRCh38
NC_000005.9:g.33951432del , CM000667.1:g.33951432del GRCh37
NC_000005.8:g.33987189del NCBI36
NG_011691.2:g.38349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1156+227del MANE Select ENSP00000296589.4:n.1156+227del
ENST00000296589.8:c.1156+227del ENSP00000296589.4:n.1156+227del
ENST00000382102.7:c.1156+227del ENSP00000371534.3:n.1156+227del
ENST00000510600.1:c.631+227del ENSP00000424010.1:n.631+227del
NM_001012509.3:c.1156+227del NP_001012527.1:n.1156+227del
NM_016180.4:c.1156+227del NP_057264.3:n.1156+227del
XM_011514051.1:c.754+227del XP_011512353.1:n.754+227del
XR_925620.1:n.1973+227del
NM_016180.5:c.1156+227del MANE Select NP_057264.4:n.1156+227del
NM_001012509.4:c.1156+227del NP_001012527.2:n.1156+227del