Canonical Allele Identifier: CA558967077
Gene: SLC45A2 HGNC NCBI

Linked Data

dbSNP Id: rs1561359853

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33955658_33955673del , CM000667.2:g.33955658_33955673del GRCh38
NC_000005.9:g.33955763_33955778del , CM000667.1:g.33955763_33955778del GRCh37
NC_000005.8:g.33991520_33991535del NCBI36
NG_011691.2:g.34018_34033del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.889-1154_889-1139del MANE Select ENSP00000296589.4:n.889-1154_889-1139del
ENST00000296589.8:c.889-1154_889-1139del ENSP00000296589.4:n.889-1154_889-1139del
ENST00000382102.7:c.889-1154_889-1139del ENSP00000371534.3:n.889-1154_889-1139del
ENST00000509381.1:c.563-1154_563-1139del ENSP00000421100.1:n.563-1154_563-1139del
ENST00000510600.1:c.364-1154_364-1139del ENSP00000424010.1:n.364-1154_364-1139del
NM_001012509.3:c.889-1154_889-1139del NP_001012527.1:n.889-1154_889-1139del
NM_001297417.2:c.563-1154_563-1139del NP_001284346.2:n.563-1154_563-1139del
NM_016180.4:c.889-1154_889-1139del NP_057264.3:n.889-1154_889-1139del
XM_011514051.1:c.487-1154_487-1139del XP_011512353.1:n.487-1154_487-1139del
XR_925620.1:n.1706-1154_1706-1139del
NM_016180.5:c.889-1154_889-1139del MANE Select NP_057264.4:n.889-1154_889-1139del
NM_001012509.4:c.889-1154_889-1139del NP_001012527.2:n.889-1154_889-1139del
NM_001297417.3:c.563-1154_563-1139del NP_001284346.2:n.563-1154_563-1139del
NM_001297417.4:c.563-1154_563-1139del NP_001284346.2:n.563-1154_563-1139del