Canonical Allele Identifier: CA1315653421
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575027G= , CM000664.2:g.189575027G= GRCh38
NC_000002.11:g.190439753G= , CM000664.1:g.190439753G= GRCh37
NC_000002.10:g.190147998G= NCBI36
NG_009027.1:g.10785C= , LRG_837:g.10785C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.271+134C= MANE Select ENSP00000261024.3:n.271+134C=
ENST00000261024.6:c.271+134C= ENSP00000261024.2:n.271+134C=
ENST00000427241.5:c.271+134C= ENSP00000390005.1:n.271+134C=
ENST00000479598.5:n.552+134C=
NM_014585.5:c.271+134C= , LRG_837t1:c.271+134C= NP_055400.1:n.271+134C=
XM_005246505.1:c.151+134C= XP_005246562.1:n.151+134C=
XM_005246505.2:c.151+134C= XP_005246562.1:n.151+134C=
XM_017003938.2:c.151+134C= XP_016859427.1:n.151+134C=
NM_014585.6:c.271+134C= MANE Select NP_055400.1:n.271+134C=