Canonical Allele Identifier: CA2765834762
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33964093_33964094insT , CM000667.2:g.33964093_33964094insT GRCh38
NC_000005.9:g.33964198_33964199insT , CM000667.1:g.33964198_33964199insT GRCh37
NC_000005.8:g.33999955_33999956insT NCBI36
NG_011691.2:g.25582_25583insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.563-78_563-77insA MANE Select ENSP00000296589.4:n.563-78_563-77insA
ENST00000296589.8:c.563-78_563-77insA ENSP00000296589.4:n.563-78_563-77insA
ENST00000382102.7:c.563-78_563-77insA ENSP00000371534.3:n.563-78_563-77insA
ENST00000505056.1:n.365-78_365-77insA
ENST00000509381.1:c.563-9590_563-9589insA ENSP00000421100.1:n.563-9590_563-9589insA
ENST00000510600.1:c.38-78_38-77insA ENSP00000424010.1:n.38-78_38-77insA
NM_001012509.3:c.563-78_563-77insA NP_001012527.1:n.563-78_563-77insA
NM_001297417.2:c.563-9590_563-9589insA NP_001284346.2:n.563-9590_563-9589insA
NM_016180.4:c.563-78_563-77insA NP_057264.3:n.563-78_563-77insA
XM_011514051.1:c.161-78_161-77insA XP_011512353.1:n.161-78_161-77insA
XM_011514052.1:c.563-78_563-77insA XP_011512354.1:n.563-78_563-77insA
XR_925620.1:n.1380-78_1380-77insA
NM_016180.5:c.563-78_563-77insA MANE Select NP_057264.4:n.563-78_563-77insA
NM_001012509.4:c.563-78_563-77insA NP_001012527.2:n.563-78_563-77insA
NM_001297417.3:c.563-9590_563-9589insA NP_001284346.2:n.563-9590_563-9589insA
NM_001297417.4:c.563-9590_563-9589insA NP_001284346.2:n.563-9590_563-9589insA