Canonical Allele Identifier: CA2482673702
Gene: SLC45A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205669043A= , CM000663.2:g.205669043A= GRCh38
NC_000001.10:g.205638171A= , CM000663.1:g.205638171A= GRCh37
NC_000001.9:g.203904794A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367145.4:c.-230-4157T= MANE Select ENSP00000356113.3:n.-230-4157T=
ENST00000367145.3:c.-230-4157T= ENSP00000356113.3:n.-230-4157T=
NM_033102.2:c.-230-4157T= NP_149093.1:n.-230-4157T=
XM_005245556.2:c.-231+652T= XP_005245613.1:n.-231+652T=
XM_005245557.3:c.-230-4157T= XP_005245614.1:n.-230-4157T=
XM_005245559.3:c.-231+2907T= XP_005245616.1:n.-231+2907T=
XM_005245560.2:c.-230-4157T= XP_005245617.1:n.-230-4157T=
NM_033102.3:c.-230-4157T= MANE Select NP_149093.1:n.-230-4157T=
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