Canonical Allele Identifier: CA1315655500
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs2030893045

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565157_189565172del , CM000664.2:g.189565157_189565172del GRCh38
NC_000002.11:g.190429883_190429898del , CM000664.1:g.190429883_190429898del GRCh37
NC_000002.10:g.190138128_190138143del NCBI36
NG_009027.1:g.20642_20657del , LRG_837:g.20642_20657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+184_760+199del MANE Select ENSP00000261024.3:n.760+184_760+199del
ENST00000261024.6:c.760+184_760+199del ENSP00000261024.2:n.760+184_760+199del
NM_014585.5:c.760+184_760+199del , LRG_837t1:c.760+184_760+199del NP_055400.1:n.760+184_760+199del
XM_005246505.1:c.640+184_640+199del XP_005246562.1:n.640+184_640+199del
XM_005246505.2:c.640+184_640+199del XP_005246562.1:n.640+184_640+199del
XM_017003938.2:c.640+184_640+199del XP_016859427.1:n.640+184_640+199del
NM_014585.6:c.760+184_760+199del MANE Select NP_055400.1:n.760+184_760+199del