Canonical Allele Identifier: CA1315650263

Gene: SLC40A1

Linked Data

• dbSNP Id: rs2031130708

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189571690_189571694del , CM000664.2:g.189571690_189571694del	GRCh38
NC_000002.11:g.190436416_190436420del , CM000664.1:g.190436416_190436420del	GRCh37
NC_000002.10:g.190144661_190144665del	NCBI36
NG_009027.1:g.14123_14127del , LRG_837:g.14123_14127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.514+26_514+30del MANE Select	ENSP00000261024.3:n.514+26_514+30del
ENST00000261024.6:c.514+26_514+30del	ENSP00000261024.2:n.514+26_514+30del
ENST00000427241.5:c.514+26_514+30del	ENSP00000390005.1:n.514+26_514+30del
NM_014585.5:c.514+26_514+30del , LRG_837t1:c.514+26_514+30del	NP_055400.1:n.514+26_514+30del
XM_005246505.1:c.394+26_394+30del	XP_005246562.1:n.394+26_394+30del
XM_005246505.2:c.394+26_394+30del	XP_005246562.1:n.394+26_394+30del
XM_017003938.2:c.394+26_394+30del	XP_016859427.1:n.394+26_394+30del
NM_014585.6:c.514+26_514+30del MANE Select	NP_055400.1:n.514+26_514+30del