Canonical Allele Identifier: CA1315654559
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564248T= , CM000664.2:g.189564248T= GRCh38
NC_000002.11:g.190428974T= , CM000664.1:g.190428974T= GRCh37
NC_000002.10:g.190137219T= NCBI36
NG_009027.1:g.21564A= , LRG_837:g.21564A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.761-23A= MANE Select ENSP00000261024.3:n.761-23A=
ENST00000261024.6:c.761-23A= ENSP00000261024.2:n.761-23A=
NM_014585.5:c.761-23A= , LRG_837t1:c.761-23A= NP_055400.1:n.761-23A=
XM_005246505.1:c.641-23A= XP_005246562.1:n.641-23A=
XM_005246505.2:c.641-23A= XP_005246562.1:n.641-23A=
XM_017003938.2:c.641-23A= XP_016859427.1:n.641-23A=
NM_014585.6:c.761-23A= MANE Select NP_055400.1:n.761-23A=