Canonical Allele Identifier: CA1538195624

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33963630_33963632delinsAAC , CM000667.2:g.33963630_33963632delinsAAC	GRCh38
NC_000005.9:g.33963735_33963737delinsAAC , CM000667.1:g.33963735_33963737delinsAAC	GRCh37
NC_000005.8:g.33999492_33999494delinsAAC	NCBI36
NG_011691.2:g.26044_26046delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.888+59_888+61delinsGTT MANE Select	ENSP00000296589.4:n.888+59_888+61delinsGTT
ENST00000296589.8:c.888+59_888+61delinsGTT	ENSP00000296589.4:n.888+59_888+61delinsGTT
ENST00000382102.7:c.888+59_888+61delinsGTT	ENSP00000371534.3:n.888+59_888+61delinsGTT
ENST00000509381.1:c.563-9128_563-9126delinsGTT	ENSP00000421100.1:n.563-9128_563-9126delinsGTT
ENST00000510600.1:c.363+59_363+61delinsGTT	ENSP00000424010.1:n.363+59_363+61delinsGTT
NM_001012509.3:c.888+59_888+61delinsGTT	NP_001012527.1:n.888+59_888+61delinsGTT
NM_001297417.2:c.563-9128_563-9126delinsGTT	NP_001284346.2:n.563-9128_563-9126delinsGTT
NM_016180.4:c.888+59_888+61delinsGTT	NP_057264.3:n.888+59_888+61delinsGTT
XM_011514051.1:c.486+59_486+61delinsGTT	XP_011512353.1:n.486+59_486+61delinsGTT
XM_011514052.1:c.888+59_888+61delinsGTT	XP_011512354.1:n.888+59_888+61delinsGTT
XR_925620.1:n.1705+59_1705+61delinsGTT
NM_016180.5:c.888+59_888+61delinsGTT MANE Select	NP_057264.4:n.888+59_888+61delinsGTT
NM_001012509.4:c.888+59_888+61delinsGTT	NP_001012527.2:n.888+59_888+61delinsGTT
NM_001297417.3:c.563-9128_563-9126delinsGTT	NP_001284346.2:n.563-9128_563-9126delinsGTT
NM_001297417.4:c.563-9128_563-9126delinsGTT	NP_001284346.2:n.563-9128_563-9126delinsGTT