Canonical Allele Identifier: CA1538218624

Gene: SLC45A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984509_33984510delinsCA , CM000667.2:g.33984509_33984510delinsCA	GRCh38
NC_000005.9:g.33984614_33984615delinsCA , CM000667.1:g.33984614_33984615delinsCA	GRCh37
NC_000005.8:g.34020371_34020372delinsCA	NCBI36
NG_011691.2:g.5166_5167delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.74_75delinsTG MANE Select	ENSP00000296589.4:p.Val25=
ENST00000296589.8:c.74_75delinsTG	ENSP00000296589.4:p.Val25=
ENST00000382102.7:c.74_75delinsTG	ENSP00000371534.3:p.Val25=
ENST00000505056.1:n.53_54delinsTG
ENST00000509381.1:c.74_75delinsTG	ENSP00000421100.1:p.Val25=
NM_001012509.3:c.74_75delinsTG	NP_001012527.1:p.Val25=
NM_001297417.2:c.74_75delinsTG	NP_001284346.2:p.Val25=
NM_016180.4:c.74_75delinsTG	NP_057264.3:p.Val25=
XM_011514052.1:c.74_75delinsTG	XP_011512354.1:p.Val25=
XR_925620.1:n.635_636delinsTG
NM_016180.5:c.74_75delinsTG MANE Select	NP_057264.4:p.Val25=
NM_001012509.4:c.74_75delinsTG	NP_001012527.2:p.Val25=
NM_001297417.3:c.74_75delinsTG	NP_001284346.2:p.Val25=
NM_001297417.4:c.74_75delinsTG	NP_001284346.2:p.Val25=