Canonical Allele Identifier: CA349988449

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190428940T>A (hg19) ; chr2:g.189564214T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564214T>A , CM000664.2:g.189564214T>A	GRCh38
NC_000002.11:g.190428940T>A , CM000664.1:g.190428940T>A	GRCh37
NC_000002.10:g.190137185T>A	NCBI36
NG_009027.1:g.21598A>T , LRG_837:g.21598A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.772A>T MANE Select	ENSP00000261024.3:p.Lys258Ter
ENST00000261024.6:c.772A>T	ENSP00000261024.2:p.Lys258Ter
NM_014585.5:c.772A>T , LRG_837t1:c.772A>T	NP_055400.1:p.Lys258Ter
XM_005246505.1:c.652A>T	XP_005246562.1:p.Lys218Ter
XM_005246505.2:c.652A>T	XP_005246562.1:p.Lys218Ter
XM_017003938.2:c.652A>T	XP_016859427.1:p.Lys218Ter
NM_014585.6:c.772A>T MANE Select	NP_055400.1:p.Lys258Ter