Canonical Allele Identifier: CA349989908

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190440037T>C (hg19) ; chr2:g.189575311T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575311T>C , CM000664.2:g.189575311T>C	GRCh38
NC_000002.11:g.190440037T>C , CM000664.1:g.190440037T>C	GRCh37
NC_000002.10:g.190148282T>C	NCBI36
NG_009027.1:g.10501A>G , LRG_837:g.10501A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.121A>G MANE Select	ENSP00000261024.3:p.Met41Val
ENST00000261024.6:c.121A>G	ENSP00000261024.2:p.Met41Val
ENST00000418714.1:n.562A>G
ENST00000427241.5:c.121A>G	ENSP00000390005.1:p.Met41Val
ENST00000455320.5:c.121A>G	ENSP00000413549.1:p.Met41Val
ENST00000479598.5:n.402A>G
NM_014585.5:c.121A>G , LRG_837t1:c.121A>G	NP_055400.1:p.Met41Val
XM_005246505.1:c.1A>G	XP_005246562.1:p.Met1Val
XM_005246505.2:c.1A>G	XP_005246562.1:p.Met1Val
XM_017003938.2:c.1A>G	XP_016859427.1:p.Met1Val
NM_014585.6:c.121A>G MANE Select	NP_055400.1:p.Met41Val