Canonical Allele Identifier: CA916735177

Gene: SLC40A1

Linked Data

• dbSNP Id: rs1559010032

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189563571del , CM000664.2:g.189563571del	GRCh38
NC_000002.11:g.190428297del , CM000664.1:g.190428297del	GRCh37
NC_000002.10:g.190136542del	NCBI36
NG_009027.1:g.22245del , LRG_837:g.22245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.1402+17del MANE Select	ENSP00000261024.3:n.1402+17del
ENST00000261024.6:c.1402+17del	ENSP00000261024.2:n.1402+17del
NM_014585.5:c.1402+17del , LRG_837t1:c.1402+17del	NP_055400.1:n.1402+17del
XM_005246505.1:c.1282+17del	XP_005246562.1:n.1282+17del
XM_005246505.2:c.1282+17del	XP_005246562.1:n.1282+17del
XM_017003938.2:c.1282+17del	XP_016859427.1:n.1282+17del
NM_014585.6:c.1402+17del MANE Select	NP_055400.1:n.1402+17del