Canonical Allele Identifier: CA349989775

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190439977T>A (hg19) ; chr2:g.189575251T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575251T>A , CM000664.2:g.189575251T>A	GRCh38
NC_000002.11:g.190439977T>A , CM000664.1:g.190439977T>A	GRCh37
NC_000002.10:g.190148222T>A	NCBI36
NG_009027.1:g.10561A>T , LRG_837:g.10561A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.181A>T MANE Select	ENSP00000261024.3:p.Thr61Ser
ENST00000261024.6:c.181A>T	ENSP00000261024.2:p.Thr61Ser
ENST00000418714.1:n.622A>T
ENST00000427241.5:c.181A>T	ENSP00000390005.1:p.Thr61Ser
ENST00000479598.5:n.462A>T
NM_014585.5:c.181A>T , LRG_837t1:c.181A>T	NP_055400.1:p.Thr61Ser
XM_005246505.1:c.61A>T	XP_005246562.1:p.Thr21Ser
XM_005246505.2:c.61A>T	XP_005246562.1:p.Thr21Ser
XM_017003938.2:c.61A>T	XP_016859427.1:p.Thr21Ser
NM_014585.6:c.181A>T MANE Select	NP_055400.1:p.Thr61Ser