Canonical Allele Identifier: CA2662329351
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571670T>G , CM000664.2:g.189571670T>G GRCh38
NC_000002.11:g.190436396T>G , CM000664.1:g.190436396T>G GRCh37
NC_000002.10:g.190144641T>G NCBI36
NG_009027.1:g.14142A>C , LRG_837:g.14142A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.514+45A>C MANE Select ENSP00000261024.3:n.514+45A>C
ENST00000261024.6:c.514+45A>C ENSP00000261024.2:n.514+45A>C
ENST00000427241.5:c.514+45A>C ENSP00000390005.1:n.514+45A>C
NM_014585.5:c.514+45A>C , LRG_837t1:c.514+45A>C NP_055400.1:n.514+45A>C
XM_005246505.1:c.394+45A>C XP_005246562.1:n.394+45A>C
XM_005246505.2:c.394+45A>C XP_005246562.1:n.394+45A>C
XM_017003938.2:c.394+45A>C XP_016859427.1:n.394+45A>C
NM_014585.6:c.514+45A>C MANE Select NP_055400.1:n.514+45A>C