Canonical Allele Identifier: CA2673477372

Gene: SLC45A2

Linked Data

• gnomAD v4: 5-33964097-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964097_33964098insAA , CM000667.2:g.33964097_33964098insAA	GRCh38
NC_000005.9:g.33964202_33964203insAA , CM000667.1:g.33964202_33964203insAA	GRCh37
NC_000005.8:g.33999959_33999960insAA	NCBI36
NG_011691.2:g.25578_25579insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-82_563-81insTT MANE Select	ENSP00000296589.4:n.563-82_563-81insTT
ENST00000296589.8:c.563-82_563-81insTT	ENSP00000296589.4:n.563-82_563-81insTT
ENST00000382102.7:c.563-82_563-81insTT	ENSP00000371534.3:n.563-82_563-81insTT
ENST00000505056.1:n.365-82_365-81insTT
ENST00000509381.1:c.563-9594_563-9593insTT	ENSP00000421100.1:n.563-9594_563-9593insTT
ENST00000510600.1:c.38-82_38-81insTT	ENSP00000424010.1:n.38-82_38-81insTT
NM_001012509.3:c.563-82_563-81insTT	NP_001012527.1:n.563-82_563-81insTT
NM_001297417.2:c.563-9594_563-9593insTT	NP_001284346.2:n.563-9594_563-9593insTT
NM_016180.4:c.563-82_563-81insTT	NP_057264.3:n.563-82_563-81insTT
XM_011514051.1:c.161-82_161-81insTT	XP_011512353.1:n.161-82_161-81insTT
XM_011514052.1:c.563-82_563-81insTT	XP_011512354.1:n.563-82_563-81insTT
XR_925620.1:n.1380-82_1380-81insTT
NM_016180.5:c.563-82_563-81insTT MANE Select	NP_057264.4:n.563-82_563-81insTT
NM_001012509.4:c.563-82_563-81insTT	NP_001012527.2:n.563-82_563-81insTT
NM_001297417.3:c.563-9594_563-9593insTT	NP_001284346.2:n.563-9594_563-9593insTT
NM_001297417.4:c.563-9594_563-9593insTT	NP_001284346.2:n.563-9594_563-9593insTT