Canonical Allele Identifier: CA349989863

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190440018G>T (hg19) ; chr2:g.189575292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575292G>T , CM000664.2:g.189575292G>T	GRCh38
NC_000002.11:g.190440018G>T , CM000664.1:g.190440018G>T	GRCh37
NC_000002.10:g.190148263G>T	NCBI36
NG_009027.1:g.10520C>A , LRG_837:g.10520C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.140C>A MANE Select	ENSP00000261024.3:p.Ser47Tyr
ENST00000261024.6:c.140C>A	ENSP00000261024.2:p.Ser47Tyr
ENST00000418714.1:n.581C>A
ENST00000427241.5:c.140C>A	ENSP00000390005.1:p.Ser47Tyr
ENST00000455320.5:c.140C>A	ENSP00000413549.1:p.Ser47Tyr
ENST00000479598.5:n.421C>A
NM_014585.5:c.140C>A , LRG_837t1:c.140C>A	NP_055400.1:p.Ser47Tyr
XM_005246505.1:c.20C>A	XP_005246562.1:p.Ser7Tyr
XM_005246505.2:c.20C>A	XP_005246562.1:p.Ser7Tyr
XM_017003938.2:c.20C>A	XP_016859427.1:p.Ser7Tyr
NM_014585.6:c.140C>A MANE Select	NP_055400.1:p.Ser47Tyr