Canonical Allele Identifier: CA1315655566
Gene: SLC40A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565224C= , CM000664.2:g.189565224C= GRCh38
NC_000002.11:g.190429950C= , CM000664.1:g.190429950C= GRCh37
NC_000002.10:g.190138195C= NCBI36
NG_009027.1:g.20588G= , LRG_837:g.20588G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+130G= MANE Select ENSP00000261024.3:n.760+130G=
ENST00000261024.6:c.760+130G= ENSP00000261024.2:n.760+130G=
NM_014585.5:c.760+130G= , LRG_837t1:c.760+130G= NP_055400.1:n.760+130G=
XM_005246505.1:c.640+130G= XP_005246562.1:n.640+130G=
XM_005246505.2:c.640+130G= XP_005246562.1:n.640+130G=
XM_017003938.2:c.640+130G= XP_016859427.1:n.640+130G=
NM_014585.6:c.760+130G= MANE Select NP_055400.1:n.760+130G=
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