Canonical Allele Identifier: CA2482673698
Gene: SLC45A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205669031C= , CM000663.2:g.205669031C= GRCh38
NC_000001.10:g.205638159C= , CM000663.1:g.205638159C= GRCh37
NC_000001.9:g.203904782C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367145.4:c.-230-4145G= MANE Select ENSP00000356113.3:n.-230-4145G=
ENST00000367145.3:c.-230-4145G= ENSP00000356113.3:n.-230-4145G=
NM_033102.2:c.-230-4145G= NP_149093.1:n.-230-4145G=
XM_005245556.2:c.-231+664G= XP_005245613.1:n.-231+664G=
XM_005245557.3:c.-230-4145G= XP_005245614.1:n.-230-4145G=
XM_005245559.3:c.-231+2919G= XP_005245616.1:n.-231+2919G=
XM_005245560.2:c.-230-4145G= XP_005245617.1:n.-230-4145G=
NM_033102.3:c.-230-4145G= MANE Select NP_149093.1:n.-230-4145G=