Canonical Allele Identifier: CA349988126

Gene: SLC40A1

Linked Data

• dbSNP Id: rs2030847694
• MyVariant Identifiers: chr2:g.190428793C>T (hg19) ; chr2:g.189564067C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564067C>T , CM000664.2:g.189564067C>T	GRCh38
NC_000002.11:g.190428793C>T , CM000664.1:g.190428793C>T	GRCh37
NC_000002.10:g.190137038C>T	NCBI36
NG_009027.1:g.21745G>A , LRG_837:g.21745G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.919G>A MANE Select	ENSP00000261024.3:p.Val307Met
ENST00000261024.6:c.919G>A	ENSP00000261024.2:p.Val307Met
NM_014585.5:c.919G>A , LRG_837t1:c.919G>A	NP_055400.1:p.Val307Met
XM_005246505.1:c.799G>A	XP_005246562.1:p.Val267Met
XM_005246505.2:c.799G>A	XP_005246562.1:p.Val267Met
XM_017003938.2:c.799G>A	XP_016859427.1:p.Val267Met
NM_014585.6:c.919G>A MANE Select	NP_055400.1:p.Val307Met