Canonical Allele Identifier: CA2673477363
Gene: SLC45A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964095_33964096insGGCG , CM000667.2:g.33964095_33964096insGGCG GRCh38
NC_000005.9:g.33964200_33964201insGGCG , CM000667.1:g.33964200_33964201insGGCG GRCh37
NC_000005.8:g.33999957_33999958insGGCG NCBI36
NG_011691.2:g.25581_25582insGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-79_563-78insGCCC MANE Select ENSP00000296589.4:n.563-79_563-78insGCCC
ENST00000296589.8:c.563-79_563-78insGCCC ENSP00000296589.4:n.563-79_563-78insGCCC
ENST00000382102.7:c.563-79_563-78insGCCC ENSP00000371534.3:n.563-79_563-78insGCCC
ENST00000505056.1:n.365-79_365-78insGCCC
ENST00000509381.1:c.563-9591_563-9590insGCCC ENSP00000421100.1:n.563-9591_563-9590insGCCC
ENST00000510600.1:c.38-79_38-78insGCCC ENSP00000424010.1:n.38-79_38-78insGCCC
NM_001012509.3:c.563-79_563-78insGCCC NP_001012527.1:n.563-79_563-78insGCCC
NM_001297417.2:c.563-9591_563-9590insGCCC NP_001284346.2:n.563-9591_563-9590insGCCC
NM_016180.4:c.563-79_563-78insGCCC NP_057264.3:n.563-79_563-78insGCCC
XM_011514051.1:c.161-79_161-78insGCCC XP_011512353.1:n.161-79_161-78insGCCC
XM_011514052.1:c.563-79_563-78insGCCC XP_011512354.1:n.563-79_563-78insGCCC
XR_925620.1:n.1380-79_1380-78insGCCC
NM_016180.5:c.563-79_563-78insGCCC MANE Select NP_057264.4:n.563-79_563-78insGCCC
NM_001012509.4:c.563-79_563-78insGCCC NP_001012527.2:n.563-79_563-78insGCCC
NM_001297417.3:c.563-9591_563-9590insGCCC NP_001284346.2:n.563-9591_563-9590insGCCC
NM_001297417.4:c.563-9591_563-9590insGCCC NP_001284346.2:n.563-9591_563-9590insGCCC