Canonical Allele Identifier: CA1315653717
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575228C= , CM000664.2:g.189575228C= GRCh38
NC_000002.11:g.190439954C= , CM000664.1:g.190439954C= GRCh37
NC_000002.10:g.190148199C= NCBI36
NG_009027.1:g.10584G= , LRG_837:g.10584G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.204G= MANE Select ENSP00000261024.3:p.Val68=
ENST00000261024.6:c.204G= ENSP00000261024.2:p.Val68=
ENST00000418714.1:n.645G=
ENST00000427241.5:c.204G= ENSP00000390005.1:p.Val68=
ENST00000479598.5:n.485G=
NM_014585.5:c.204G= , LRG_837t1:c.204G= NP_055400.1:p.Val68=
XM_005246505.1:c.84G= XP_005246562.1:p.Val28=
XM_005246505.2:c.84G= XP_005246562.1:p.Val28=
XM_017003938.2:c.84G= XP_016859427.1:p.Val28=
NM_014585.6:c.204G= MANE Select NP_055400.1:p.Val68=