Canonical Allele Identifier: CA1538185445
Gene: SLC45A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33955783_33955786delinsTGAA , CM000667.2:g.33955783_33955786delinsTGAA GRCh38
NC_000005.9:g.33955888_33955891delinsTGAA , CM000667.1:g.33955888_33955891delinsTGAA GRCh37
NC_000005.8:g.33991645_33991648delinsTGAA NCBI36
NG_011691.2:g.33890_33893delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.889-1282_889-1279delinsTTCA MANE Select ENSP00000296589.4:n.889-1282_889-1279delinsTTCA
ENST00000296589.8:c.889-1282_889-1279delinsTTCA ENSP00000296589.4:n.889-1282_889-1279delinsTTCA
ENST00000382102.7:c.889-1282_889-1279delinsTTCA ENSP00000371534.3:n.889-1282_889-1279delinsTTCA
ENST00000509381.1:c.563-1282_563-1279delinsTTCA ENSP00000421100.1:n.563-1282_563-1279delinsTTCA
ENST00000510600.1:c.364-1282_364-1279delinsTTCA ENSP00000424010.1:n.364-1282_364-1279delinsTTCA
NM_001012509.3:c.889-1282_889-1279delinsTTCA NP_001012527.1:n.889-1282_889-1279delinsTTCA
NM_001297417.2:c.563-1282_563-1279delinsTTCA NP_001284346.2:n.563-1282_563-1279delinsTTCA
NM_016180.4:c.889-1282_889-1279delinsTTCA NP_057264.3:n.889-1282_889-1279delinsTTCA
XM_011514051.1:c.487-1282_487-1279delinsTTCA XP_011512353.1:n.487-1282_487-1279delinsTTCA
XR_925620.1:n.1706-1282_1706-1279delinsTTCA
NM_016180.5:c.889-1282_889-1279delinsTTCA MANE Select NP_057264.4:n.889-1282_889-1279delinsTTCA
NM_001012509.4:c.889-1282_889-1279delinsTTCA NP_001012527.2:n.889-1282_889-1279delinsTTCA
NM_001297417.3:c.563-1282_563-1279delinsTTCA NP_001284346.2:n.563-1282_563-1279delinsTTCA
NM_001297417.4:c.563-1282_563-1279delinsTTCA NP_001284346.2:n.563-1282_563-1279delinsTTCA