Canonical Allele Identifier: CA349989849

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190440012A>C (hg19) ; chr2:g.189575286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575286A>C , CM000664.2:g.189575286A>C	GRCh38
NC_000002.11:g.190440012A>C , CM000664.1:g.190440012A>C	GRCh37
NC_000002.10:g.190148257A>C	NCBI36
NG_009027.1:g.10526T>G , LRG_837:g.10526T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.146T>G MANE Select	ENSP00000261024.3:p.Phe49Cys
ENST00000261024.6:c.146T>G	ENSP00000261024.2:p.Phe49Cys
ENST00000418714.1:n.587T>G
ENST00000427241.5:c.146T>G	ENSP00000390005.1:p.Phe49Cys
ENST00000455320.5:c.146T>G	ENSP00000413549.1:p.Phe49Cys
ENST00000479598.5:n.427T>G
NM_014585.5:c.146T>G , LRG_837t1:c.146T>G	NP_055400.1:p.Phe49Cys
XM_005246505.1:c.26T>G	XP_005246562.1:p.Phe9Cys
XM_005246505.2:c.26T>G	XP_005246562.1:p.Phe9Cys
XM_017003938.2:c.26T>G	XP_016859427.1:p.Phe9Cys
NM_014585.6:c.146T>G MANE Select	NP_055400.1:p.Phe49Cys