Canonical Allele Identifier: CA36465350

Gene: SLC45A3

Linked Data

• dbSNP Id: rs36123633
• MyVariant Identifiers: chr1:g.205638357_205638358insC (hg19) ; chr1:g.205669229_205669230insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205669231dup , CM000663.2:g.205669231dup	GRCh38
NC_000001.10:g.205638359dup , CM000663.1:g.205638359dup	GRCh37
NC_000001.9:g.203904982dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367145.4:c.-230-4344dup MANE Select	ENSP00000356113.3:n.-230-4344dup
ENST00000367145.3:c.-230-4344dup	ENSP00000356113.3:n.-230-4344dup
NM_033102.2:c.-230-4344dup	NP_149093.1:n.-230-4344dup
XM_005245556.2:c.-231+465dup	XP_005245613.1:n.-231+465dup
XM_005245557.3:c.-230-4344dup	XP_005245614.1:n.-230-4344dup
XM_005245559.3:c.-231+2720dup	XP_005245616.1:n.-231+2720dup
XM_005245560.2:c.-230-4344dup	XP_005245617.1:n.-230-4344dup
NM_033102.3:c.-230-4344dup MANE Select	NP_149093.1:n.-230-4344dup