Canonical Allele Identifier: CA349988173
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs1448569115

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564088C>A , CM000664.2:g.189564088C>A GRCh38
NC_000002.11:g.190428814C>A , CM000664.1:g.190428814C>A GRCh37
NC_000002.10:g.190137059C>A NCBI36
NG_009027.1:g.21724G>T , LRG_837:g.21724G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.898G>T MANE Select ENSP00000261024.3:p.Val300Phe
ENST00000261024.6:c.898G>T ENSP00000261024.2:p.Val300Phe
NM_014585.5:c.898G>T , LRG_837t1:c.898G>T NP_055400.1:p.Val300Phe
XM_005246505.1:c.778G>T XP_005246562.1:p.Val260Phe
XM_005246505.2:c.778G>T XP_005246562.1:p.Val260Phe
XM_017003938.2:c.778G>T XP_016859427.1:p.Val260Phe
NM_014585.6:c.898G>T MANE Select NP_055400.1:p.Val300Phe