Canonical Allele Identifier: CA1315655639
Gene: SLC40A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565318T= , CM000664.2:g.189565318T= GRCh38
NC_000002.11:g.190430044T= , CM000664.1:g.190430044T= GRCh37
NC_000002.10:g.190138289T= NCBI36
NG_009027.1:g.20494A= , LRG_837:g.20494A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.760+36A= MANE Select ENSP00000261024.3:n.760+36A=
ENST00000261024.6:c.760+36A= ENSP00000261024.2:n.760+36A=
NM_014585.5:c.760+36A= , LRG_837t1:c.760+36A= NP_055400.1:n.760+36A=
XM_005246505.1:c.640+36A= XP_005246562.1:n.640+36A=
XM_005246505.2:c.640+36A= XP_005246562.1:n.640+36A=
XM_017003938.2:c.640+36A= XP_016859427.1:n.640+36A=
NM_014585.6:c.760+36A= MANE Select NP_055400.1:n.760+36A=
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