Canonical Allele Identifier: CA349989595

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190439887C>T (hg19) ; chr2:g.189575161C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575161C>T , CM000664.2:g.189575161C>T	GRCh38
NC_000002.11:g.190439887C>T , CM000664.1:g.190439887C>T	GRCh37
NC_000002.10:g.190148132C>T	NCBI36
NG_009027.1:g.10651G>A , LRG_837:g.10651G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.271G>A MANE Select	ENSP00000261024.3:p.Val91Met
ENST00000261024.6:c.271G>A	ENSP00000261024.2:p.Val91Met
ENST00000418714.1:n.712G>A
ENST00000427241.5:c.271G>A	ENSP00000390005.1:p.Val91Met
ENST00000479598.5:n.552G>A
NM_014585.5:c.271G>A , LRG_837t1:c.271G>A	NP_055400.1:p.Val91Met
XM_005246505.1:c.151G>A	XP_005246562.1:p.Val51Met
XM_005246505.2:c.151G>A	XP_005246562.1:p.Val51Met
XM_017003938.2:c.151G>A	XP_016859427.1:p.Val51Met
NM_014585.6:c.271G>A MANE Select	NP_055400.1:p.Val91Met