Canonical Allele Identifier: CA2555749711

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33955671_33955676dup , CM000667.2:g.33955671_33955676dup	GRCh38
NC_000005.9:g.33955776_33955781dup , CM000667.1:g.33955776_33955781dup	GRCh37
NC_000005.8:g.33991533_33991538dup	NCBI36
NG_011691.2:g.34012_34017dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-1160_889-1155dup MANE Select	ENSP00000296589.4:n.889-1160_889-1155dup
ENST00000296589.8:c.889-1160_889-1155dup	ENSP00000296589.4:n.889-1160_889-1155dup
ENST00000382102.7:c.889-1160_889-1155dup	ENSP00000371534.3:n.889-1160_889-1155dup
ENST00000509381.1:c.563-1160_563-1155dup	ENSP00000421100.1:n.563-1160_563-1155dup
ENST00000510600.1:c.364-1160_364-1155dup	ENSP00000424010.1:n.364-1160_364-1155dup
NM_001012509.3:c.889-1160_889-1155dup	NP_001012527.1:n.889-1160_889-1155dup
NM_001297417.2:c.563-1160_563-1155dup	NP_001284346.2:n.563-1160_563-1155dup
NM_016180.4:c.889-1160_889-1155dup	NP_057264.3:n.889-1160_889-1155dup
XM_011514051.1:c.487-1160_487-1155dup	XP_011512353.1:n.487-1160_487-1155dup
XR_925620.1:n.1706-1160_1706-1155dup
NM_016180.5:c.889-1160_889-1155dup MANE Select	NP_057264.4:n.889-1160_889-1155dup
NM_001012509.4:c.889-1160_889-1155dup	NP_001012527.2:n.889-1160_889-1155dup
NM_001297417.3:c.563-1160_563-1155dup	NP_001284346.2:n.563-1160_563-1155dup
NM_001297417.4:c.563-1160_563-1155dup	NP_001284346.2:n.563-1160_563-1155dup