Canonical Allele Identifier: CA1074904351

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1752532171
• gnomAD v3: 5-33964103-A-ACGC
• gnomAD v4: 5-33964103-A-ACGC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33964104_33964105insGCC , CM000667.2:g.33964104_33964105insGCC	GRCh38
NC_000005.9:g.33964209_33964210insGCC , CM000667.1:g.33964209_33964210insGCC	GRCh37
NC_000005.8:g.33999966_33999967insGCC	NCBI36
NG_011691.2:g.25572_25573insGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.563-88_563-87insGCG MANE Select	ENSP00000296589.4:n.563-88_563-87insGCG
ENST00000296589.8:c.563-88_563-87insGCG	ENSP00000296589.4:n.563-88_563-87insGCG
ENST00000382102.7:c.563-88_563-87insGCG	ENSP00000371534.3:n.563-88_563-87insGCG
ENST00000505056.1:n.365-88_365-87insGCG
ENST00000509381.1:c.563-9600_563-9599insGCG	ENSP00000421100.1:n.563-9600_563-9599insGCG
ENST00000510600.1:c.38-88_38-87insGCG	ENSP00000424010.1:n.38-88_38-87insGCG
NM_001012509.3:c.563-88_563-87insGCG	NP_001012527.1:n.563-88_563-87insGCG
NM_001297417.2:c.563-9600_563-9599insGCG	NP_001284346.2:n.563-9600_563-9599insGCG
NM_016180.4:c.563-88_563-87insGCG	NP_057264.3:n.563-88_563-87insGCG
XM_011514051.1:c.161-88_161-87insGCG	XP_011512353.1:n.161-88_161-87insGCG
XM_011514052.1:c.563-88_563-87insGCG	XP_011512354.1:n.563-88_563-87insGCG
XR_925620.1:n.1380-88_1380-87insGCG
NM_016180.5:c.563-88_563-87insGCG MANE Select	NP_057264.4:n.563-88_563-87insGCG
NM_001012509.4:c.563-88_563-87insGCG	NP_001012527.2:n.563-88_563-87insGCG
NM_001297417.3:c.563-9600_563-9599insGCG	NP_001284346.2:n.563-9600_563-9599insGCG
NM_001297417.4:c.563-9600_563-9599insGCG	NP_001284346.2:n.563-9600_563-9599insGCG