Canonical Allele Identifier: CA2765834691

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964074_33964075insAG , CM000667.2:g.33964074_33964075insAG	GRCh38
NC_000005.9:g.33964179_33964180insAG , CM000667.1:g.33964179_33964180insAG	GRCh37
NC_000005.8:g.33999936_33999937insAG	NCBI36
NG_011691.2:g.25601_25602insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-59_563-58insCT MANE Select	ENSP00000296589.4:n.563-59_563-58insCT
ENST00000296589.8:c.563-59_563-58insCT	ENSP00000296589.4:n.563-59_563-58insCT
ENST00000382102.7:c.563-59_563-58insCT	ENSP00000371534.3:n.563-59_563-58insCT
ENST00000505056.1:n.365-59_365-58insCT
ENST00000509381.1:c.563-9571_563-9570insCT	ENSP00000421100.1:n.563-9571_563-9570insCT
ENST00000510600.1:c.38-59_38-58insCT	ENSP00000424010.1:n.38-59_38-58insCT
NM_001012509.3:c.563-59_563-58insCT	NP_001012527.1:n.563-59_563-58insCT
NM_001297417.2:c.563-9571_563-9570insCT	NP_001284346.2:n.563-9571_563-9570insCT
NM_016180.4:c.563-59_563-58insCT	NP_057264.3:n.563-59_563-58insCT
XM_011514051.1:c.161-59_161-58insCT	XP_011512353.1:n.161-59_161-58insCT
XM_011514052.1:c.563-59_563-58insCT	XP_011512354.1:n.563-59_563-58insCT
XR_925620.1:n.1380-59_1380-58insCT
NM_016180.5:c.563-59_563-58insCT MANE Select	NP_057264.4:n.563-59_563-58insCT
NM_001012509.4:c.563-59_563-58insCT	NP_001012527.2:n.563-59_563-58insCT
NM_001297417.3:c.563-9571_563-9570insCT	NP_001284346.2:n.563-9571_563-9570insCT
NM_001297417.4:c.563-9571_563-9570insCT	NP_001284346.2:n.563-9571_563-9570insCT