Canonical Allele Identifier: CA1315654458
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564165T= , CM000664.2:g.189564165T= GRCh38
NC_000002.11:g.190428891T= , CM000664.1:g.190428891T= GRCh37
NC_000002.10:g.190137136T= NCBI36
NG_009027.1:g.21647A= , LRG_837:g.21647A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.821A= MANE Select ENSP00000261024.3:p.His274=
ENST00000261024.6:c.821A= ENSP00000261024.2:p.His274=
NM_014585.5:c.821A= , LRG_837t1:c.821A= NP_055400.1:p.His274=
XM_005246505.1:c.701A= XP_005246562.1:p.His234=
XM_005246505.2:c.701A= XP_005246562.1:p.His234=
XM_017003938.2:c.701A= XP_016859427.1:p.His234=
NM_014585.6:c.821A= MANE Select NP_055400.1:p.His274=