Canonical Allele Identifier: CA349989926

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190440046C>T (hg19) ; chr2:g.189575320C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575320C>T , CM000664.2:g.189575320C>T	GRCh38
NC_000002.11:g.190440046C>T , CM000664.1:g.190440046C>T	GRCh37
NC_000002.10:g.190148291C>T	NCBI36
NG_009027.1:g.10492G>A , LRG_837:g.10492G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112G>A MANE Select	ENSP00000261024.3:p.Gly38Arg
ENST00000261024.6:c.112G>A	ENSP00000261024.2:p.Gly38Arg
ENST00000418714.1:n.553G>A
ENST00000427241.5:c.112G>A	ENSP00000390005.1:p.Gly38Arg
ENST00000455320.5:c.112G>A	ENSP00000413549.1:p.Gly38Arg
ENST00000479598.5:n.393G>A
NM_014585.5:c.112G>A , LRG_837t1:c.112G>A	NP_055400.1:p.Gly38Arg
XM_005246505.1:c.-9G>A	XP_005246562.1:n.-9G>A
XM_005246505.2:c.-9G>A	XP_005246562.1:n.-9G>A
XM_017003938.2:c.-9G>A	XP_016859427.1:n.-9G>A
NM_014585.6:c.112G>A MANE Select	NP_055400.1:p.Gly38Arg