Canonical Allele Identifier: CA1538218617
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33984495_33984498delinsCTTT , CM000667.2:g.33984495_33984498delinsCTTT GRCh38
NC_000005.9:g.33984600_33984603delinsCTTT , CM000667.1:g.33984600_33984603delinsCTTT GRCh37
NC_000005.8:g.34020357_34020360delinsCTTT NCBI36
NG_011691.2:g.5178_5181delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.86_89delinsAAAG MANE Select ENSP00000296589.4:p.Lys29=
ENST00000296589.8:c.86_89delinsAAAG ENSP00000296589.4:p.Lys29=
ENST00000382102.7:c.86_89delinsAAAG ENSP00000371534.3:p.Lys29=
ENST00000505056.1:n.65_68delinsAAAG
ENST00000509381.1:c.86_89delinsAAAG ENSP00000421100.1:p.Lys29=
NM_001012509.3:c.86_89delinsAAAG NP_001012527.1:p.Lys29=
NM_001297417.2:c.86_89delinsAAAG NP_001284346.2:p.Lys29=
NM_016180.4:c.86_89delinsAAAG NP_057264.3:p.Lys29=
XM_011514052.1:c.86_89delinsAAAG XP_011512354.1:p.Lys29=
XR_925620.1:n.647_650delinsAAAG
NM_016180.5:c.86_89delinsAAAG MANE Select NP_057264.4:p.Lys29=
NM_001012509.4:c.86_89delinsAAAG NP_001012527.2:p.Lys29=
NM_001297417.3:c.86_89delinsAAAG NP_001284346.2:p.Lys29=
NM_001297417.4:c.86_89delinsAAAG NP_001284346.2:p.Lys29=