Canonical Allele Identifier: CA349988598
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565401C>T , CM000664.2:g.189565401C>T GRCh38
NC_000002.11:g.190430127C>T , CM000664.1:g.190430127C>T GRCh37
NC_000002.10:g.190138372C>T NCBI36
NG_009027.1:g.20411G>A , LRG_837:g.20411G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.713G>A MANE Select ENSP00000261024.3:p.Gly238Asp
ENST00000261024.6:c.713G>A ENSP00000261024.2:p.Gly238Asp
NM_014585.5:c.713G>A , LRG_837t1:c.713G>A NP_055400.1:p.Gly238Asp
XM_005246505.1:c.593G>A XP_005246562.1:p.Gly198Asp
XM_005246505.2:c.593G>A XP_005246562.1:p.Gly198Asp
XM_017003938.2:c.593G>A XP_016859427.1:p.Gly198Asp
NM_014585.6:c.713G>A MANE Select NP_055400.1:p.Gly238Asp