Canonical Allele Identifier: CA1315650304
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571722T= , CM000664.2:g.189571722T= GRCh38
NC_000002.11:g.190436448T= , CM000664.1:g.190436448T= GRCh37
NC_000002.10:g.190144693T= NCBI36
NG_009027.1:g.14090A= , LRG_837:g.14090A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.507A= MANE Select ENSP00000261024.3:p.Lys169=
ENST00000261024.6:c.507A= ENSP00000261024.2:p.Lys169=
ENST00000427241.5:c.507A= ENSP00000390005.1:p.Lys169=
NM_014585.5:c.507A= , LRG_837t1:c.507A= NP_055400.1:p.Lys169=
XM_005246505.1:c.387A= XP_005246562.1:p.Lys129=
XM_005246505.2:c.387A= XP_005246562.1:p.Lys129=
XM_017003938.2:c.387A= XP_016859427.1:p.Lys129=
NM_014585.6:c.507A= MANE Select NP_055400.1:p.Lys169=