Canonical Allele Identifier: CA1315654527
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564214T= , CM000664.2:g.189564214T= GRCh38
NC_000002.11:g.190428940T= , CM000664.1:g.190428940T= GRCh37
NC_000002.10:g.190137185T= NCBI36
NG_009027.1:g.21598A= , LRG_837:g.21598A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.772A= MANE Select ENSP00000261024.3:p.Lys258=
ENST00000261024.6:c.772A= ENSP00000261024.2:p.Lys258=
NM_014585.5:c.772A= , LRG_837t1:c.772A= NP_055400.1:p.Lys258=
XM_005246505.1:c.652A= XP_005246562.1:p.Lys218=
XM_005246505.2:c.652A= XP_005246562.1:p.Lys218=
XM_017003938.2:c.652A= XP_016859427.1:p.Lys218=
NM_014585.6:c.772A= MANE Select NP_055400.1:p.Lys258=