Canonical Allele Identifier: CA1538189275

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958518_33958519delinsAT , CM000667.2:g.33958518_33958519delinsAT	GRCh38
NC_000005.9:g.33958623_33958624delinsAT , CM000667.1:g.33958623_33958624delinsAT	GRCh37
NC_000005.8:g.33994380_33994381delinsAT	NCBI36
NG_011691.2:g.31157_31158delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4015_889-4014delinsAT MANE Select	ENSP00000296589.4:n.889-4015_889-4014delinsAT
ENST00000296589.8:c.889-4015_889-4014delinsAT	ENSP00000296589.4:n.889-4015_889-4014delinsAT
ENST00000382102.7:c.889-4015_889-4014delinsAT	ENSP00000371534.3:n.889-4015_889-4014delinsAT
ENST00000509381.1:c.563-4015_563-4014delinsAT	ENSP00000421100.1:n.563-4015_563-4014delinsAT
ENST00000510600.1:c.364-4015_364-4014delinsAT	ENSP00000424010.1:n.364-4015_364-4014delinsAT
NM_001012509.3:c.889-4015_889-4014delinsAT	NP_001012527.1:n.889-4015_889-4014delinsAT
NM_001297417.2:c.563-4015_563-4014delinsAT	NP_001284346.2:n.563-4015_563-4014delinsAT
NM_016180.4:c.889-4015_889-4014delinsAT	NP_057264.3:n.889-4015_889-4014delinsAT
XM_011514051.1:c.487-4015_487-4014delinsAT	XP_011512353.1:n.487-4015_487-4014delinsAT
XR_925620.1:n.1706-4015_1706-4014delinsAT
NM_016180.5:c.889-4015_889-4014delinsAT MANE Select	NP_057264.4:n.889-4015_889-4014delinsAT
NM_001012509.4:c.889-4015_889-4014delinsAT	NP_001012527.2:n.889-4015_889-4014delinsAT
NM_001297417.3:c.563-4015_563-4014delinsAT	NP_001284346.2:n.563-4015_563-4014delinsAT
NM_001297417.4:c.563-4015_563-4014delinsAT	NP_001284346.2:n.563-4015_563-4014delinsAT