Canonical Allele Identifier: CA1315653726
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189575240G= , CM000664.2:g.189575240G= GRCh38
NC_000002.11:g.190439966G= , CM000664.1:g.190439966G= GRCh37
NC_000002.10:g.190148211G= NCBI36
NG_009027.1:g.10572C= , LRG_837:g.10572C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.192C= MANE Select ENSP00000261024.3:p.Tyr64=
ENST00000261024.6:c.192C= ENSP00000261024.2:p.Tyr64=
ENST00000418714.1:n.633C=
ENST00000427241.5:c.192C= ENSP00000390005.1:p.Tyr64=
ENST00000479598.5:n.473C=
NM_014585.5:c.192C= , LRG_837t1:c.192C= NP_055400.1:p.Tyr64=
XM_005246505.1:c.72C= XP_005246562.1:p.Tyr24=
XM_005246505.2:c.72C= XP_005246562.1:p.Tyr24=
XM_017003938.2:c.72C= XP_016859427.1:p.Tyr24=
NM_014585.6:c.192C= MANE Select NP_055400.1:p.Tyr64=