Canonical Allele Identifier: CA1315650254
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571682T= , CM000664.2:g.189571682T= GRCh38
NC_000002.11:g.190436408T= , CM000664.1:g.190436408T= GRCh37
NC_000002.10:g.190144653T= NCBI36
NG_009027.1:g.14130A= , LRG_837:g.14130A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.514+33A= MANE Select ENSP00000261024.3:n.514+33A=
ENST00000261024.6:c.514+33A= ENSP00000261024.2:n.514+33A=
ENST00000427241.5:c.514+33A= ENSP00000390005.1:n.514+33A=
NM_014585.5:c.514+33A= , LRG_837t1:c.514+33A= NP_055400.1:n.514+33A=
XM_005246505.1:c.394+33A= XP_005246562.1:n.394+33A=
XM_005246505.2:c.394+33A= XP_005246562.1:n.394+33A=
XM_017003938.2:c.394+33A= XP_016859427.1:n.394+33A=
NM_014585.6:c.514+33A= MANE Select NP_055400.1:n.514+33A=