Canonical Allele Identifier: CA1315653431
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575037C= , CM000664.2:g.189575037C= GRCh38
NC_000002.11:g.190439763C= , CM000664.1:g.190439763C= GRCh37
NC_000002.10:g.190148008C= NCBI36
NG_009027.1:g.10775G= , LRG_837:g.10775G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.271+124G= MANE Select ENSP00000261024.3:n.271+124G=
ENST00000261024.6:c.271+124G= ENSP00000261024.2:n.271+124G=
ENST00000427241.5:c.271+124G= ENSP00000390005.1:n.271+124G=
ENST00000479598.5:n.552+124G=
NM_014585.5:c.271+124G= , LRG_837t1:c.271+124G= NP_055400.1:n.271+124G=
XM_005246505.1:c.151+124G= XP_005246562.1:n.151+124G=
XM_005246505.2:c.151+124G= XP_005246562.1:n.151+124G=
XM_017003938.2:c.151+124G= XP_016859427.1:n.151+124G=
NM_014585.6:c.271+124G= MANE Select NP_055400.1:n.271+124G=