Canonical Allele Identifier: CA2662329016
Gene: SLC40A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575026del , CM000664.2:g.189575026del GRCh38
NC_000002.11:g.190439752del , CM000664.1:g.190439752del GRCh37
NC_000002.10:g.190147997del NCBI36
NG_009027.1:g.10787del , LRG_837:g.10787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.271+136del MANE Select ENSP00000261024.3:n.271+136del
ENST00000261024.6:c.271+136del ENSP00000261024.2:n.271+136del
ENST00000427241.5:c.271+136del ENSP00000390005.1:n.271+136del
ENST00000479598.5:n.552+136del
NM_014585.5:c.271+136del , LRG_837t1:c.271+136del NP_055400.1:n.271+136del
XM_005246505.1:c.151+136del XP_005246562.1:n.151+136del
XM_005246505.2:c.151+136del XP_005246562.1:n.151+136del
XM_017003938.2:c.151+136del XP_016859427.1:n.151+136del
NM_014585.6:c.271+136del MANE Select NP_055400.1:n.271+136del