Canonical Allele Identifier: CA430502815

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190428935G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564209G>C , CM000664.2:g.189564209G>C	GRCh38
NC_000002.11:g.190428935G>C , CM000664.1:g.190428935G>C	GRCh37
NC_000002.10:g.190137180G>C	NCBI36
NG_009027.1:g.21603C>G , LRG_837:g.21603C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.777C>G MANE Select	ENSP00000261024.3:p.Pro259=
ENST00000261024.6:c.777C>G	ENSP00000261024.2:p.Pro259=
NM_014585.5:c.777C>G , LRG_837t1:c.777C>G	NP_055400.1:p.Pro259=
XM_005246505.1:c.657C>G	XP_005246562.1:p.Pro219=
XM_005246505.2:c.657C>G	XP_005246562.1:p.Pro219=
XM_017003938.2:c.657C>G	XP_016859427.1:p.Pro219=
NM_014585.6:c.777C>G MANE Select	NP_055400.1:p.Pro259=