Canonical Allele Identifier: CA2765834837

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951754_33951759del , CM000667.2:g.33951754_33951759del	GRCh38
NC_000005.9:g.33951859_33951864del , CM000667.1:g.33951859_33951864del	GRCh37
NC_000005.8:g.33987616_33987621del	NCBI36
NG_011691.2:g.37917_37922del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1033-82_1033-77del MANE Select	ENSP00000296589.4:n.1033-82_1033-77del
ENST00000296589.8:c.1033-82_1033-77del	ENSP00000296589.4:n.1033-82_1033-77del
ENST00000382102.7:c.1033-82_1033-77del	ENSP00000371534.3:n.1033-82_1033-77del
ENST00000509381.1:c.707-82_707-77del	ENSP00000421100.1:n.707-82_707-77del
ENST00000510600.1:c.508-82_508-77del	ENSP00000424010.1:n.508-82_508-77del
NM_001012509.3:c.1033-82_1033-77del	NP_001012527.1:n.1033-82_1033-77del
NM_001297417.2:c.707-82_707-77del	NP_001284346.2:n.707-82_707-77del
NM_016180.4:c.1033-82_1033-77del	NP_057264.3:n.1033-82_1033-77del
XM_011514051.1:c.631-82_631-77del	XP_011512353.1:n.631-82_631-77del
XR_925620.1:n.1850-82_1850-77del
NM_016180.5:c.1033-82_1033-77del MANE Select	NP_057264.4:n.1033-82_1033-77del
NM_001012509.4:c.1033-82_1033-77del	NP_001012527.2:n.1033-82_1033-77del
NM_001297417.3:c.707-82_707-77del	NP_001284346.2:n.707-82_707-77del
NM_001297417.4:c.707-82_707-77del	NP_001284346.2:n.707-82_707-77del