Canonical Allele Identifier: CA1538189382

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33958615_33958616delinsCA , CM000667.2:g.33958615_33958616delinsCA	GRCh38
NC_000005.9:g.33958720_33958721delinsCA , CM000667.1:g.33958720_33958721delinsCA	GRCh37
NC_000005.8:g.33994477_33994478delinsCA	NCBI36
NG_011691.2:g.31060_31061delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-4112_889-4111delinsTG MANE Select	ENSP00000296589.4:n.889-4112_889-4111delinsTG
ENST00000296589.8:c.889-4112_889-4111delinsTG	ENSP00000296589.4:n.889-4112_889-4111delinsTG
ENST00000382102.7:c.889-4112_889-4111delinsTG	ENSP00000371534.3:n.889-4112_889-4111delinsTG
ENST00000509381.1:c.563-4112_563-4111delinsTG	ENSP00000421100.1:n.563-4112_563-4111delinsTG
ENST00000510600.1:c.364-4112_364-4111delinsTG	ENSP00000424010.1:n.364-4112_364-4111delinsTG
NM_001012509.3:c.889-4112_889-4111delinsTG	NP_001012527.1:n.889-4112_889-4111delinsTG
NM_001297417.2:c.563-4112_563-4111delinsTG	NP_001284346.2:n.563-4112_563-4111delinsTG
NM_016180.4:c.889-4112_889-4111delinsTG	NP_057264.3:n.889-4112_889-4111delinsTG
XM_011514051.1:c.487-4112_487-4111delinsTG	XP_011512353.1:n.487-4112_487-4111delinsTG
XR_925620.1:n.1706-4112_1706-4111delinsTG
NM_016180.5:c.889-4112_889-4111delinsTG MANE Select	NP_057264.4:n.889-4112_889-4111delinsTG
NM_001012509.4:c.889-4112_889-4111delinsTG	NP_001012527.2:n.889-4112_889-4111delinsTG
NM_001297417.3:c.563-4112_563-4111delinsTG	NP_001284346.2:n.563-4112_563-4111delinsTG
NM_001297417.4:c.563-4112_563-4111delinsTG	NP_001284346.2:n.563-4112_563-4111delinsTG