Canonical Allele Identifier: CA1315650292
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189571709A= , CM000664.2:g.189571709A= GRCh38
NC_000002.11:g.190436435A= , CM000664.1:g.190436435A= GRCh37
NC_000002.10:g.190144680A= NCBI36
NG_009027.1:g.14103T= , LRG_837:g.14103T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.514+6T= MANE Select ENSP00000261024.3:n.514+6T=
ENST00000261024.6:c.514+6T= ENSP00000261024.2:n.514+6T=
ENST00000427241.5:c.514+6T= ENSP00000390005.1:n.514+6T=
NM_014585.5:c.514+6T= , LRG_837t1:c.514+6T= NP_055400.1:n.514+6T=
XM_005246505.1:c.394+6T= XP_005246562.1:n.394+6T=
XM_005246505.2:c.394+6T= XP_005246562.1:n.394+6T=
XM_017003938.2:c.394+6T= XP_016859427.1:n.394+6T=
NM_014585.6:c.514+6T= MANE Select NP_055400.1:n.514+6T=