Canonical Allele Identifier: CA1315653739
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563510T= , CM000664.2:g.189563510T= GRCh38
NC_000002.11:g.190428236T= , CM000664.1:g.190428236T= GRCh37
NC_000002.10:g.190136481T= NCBI36
NG_009027.1:g.22302A= , LRG_837:g.22302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+74A= MANE Select ENSP00000261024.3:n.1402+74A=
ENST00000261024.6:c.1402+74A= ENSP00000261024.2:n.1402+74A=
NM_014585.5:c.1402+74A= , LRG_837t1:c.1402+74A= NP_055400.1:n.1402+74A=
XM_005246505.1:c.1282+74A= XP_005246562.1:n.1282+74A=
XM_005246505.2:c.1282+74A= XP_005246562.1:n.1282+74A=
XM_017003938.2:c.1282+74A= XP_016859427.1:n.1282+74A=
NM_014585.6:c.1402+74A= MANE Select NP_055400.1:n.1402+74A=