Canonical Allele Identifier: CA1538189575

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958758_33958760delinsCGT , CM000667.2:g.33958758_33958760delinsCGT	GRCh38
NC_000005.9:g.33958863_33958865delinsCGT , CM000667.1:g.33958863_33958865delinsCGT	GRCh37
NC_000005.8:g.33994620_33994622delinsCGT	NCBI36
NG_011691.2:g.30916_30918delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4256_889-4254delinsACG MANE Select	ENSP00000296589.4:n.889-4256_889-4254delinsACG
ENST00000296589.8:c.889-4256_889-4254delinsACG	ENSP00000296589.4:n.889-4256_889-4254delinsACG
ENST00000382102.7:c.889-4256_889-4254delinsACG	ENSP00000371534.3:n.889-4256_889-4254delinsACG
ENST00000509381.1:c.563-4256_563-4254delinsACG	ENSP00000421100.1:n.563-4256_563-4254delinsACG
ENST00000510600.1:c.364-4256_364-4254delinsACG	ENSP00000424010.1:n.364-4256_364-4254delinsACG
NM_001012509.3:c.889-4256_889-4254delinsACG	NP_001012527.1:n.889-4256_889-4254delinsACG
NM_001297417.2:c.563-4256_563-4254delinsACG	NP_001284346.2:n.563-4256_563-4254delinsACG
NM_016180.4:c.889-4256_889-4254delinsACG	NP_057264.3:n.889-4256_889-4254delinsACG
XM_011514051.1:c.487-4256_487-4254delinsACG	XP_011512353.1:n.487-4256_487-4254delinsACG
XR_925620.1:n.1706-4256_1706-4254delinsACG
NM_016180.5:c.889-4256_889-4254delinsACG MANE Select	NP_057264.4:n.889-4256_889-4254delinsACG
NM_001012509.4:c.889-4256_889-4254delinsACG	NP_001012527.2:n.889-4256_889-4254delinsACG
NM_001297417.3:c.563-4256_563-4254delinsACG	NP_001284346.2:n.563-4256_563-4254delinsACG
NM_001297417.4:c.563-4256_563-4254delinsACG	NP_001284346.2:n.563-4256_563-4254delinsACG