Canonical Allele Identifier: CA1315645017
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189565529A= , CM000664.2:g.189565529A= GRCh38
NC_000002.11:g.190430255A= , CM000664.1:g.190430255A= GRCh37
NC_000002.10:g.190138500A= NCBI36
NG_009027.1:g.20283T= , LRG_837:g.20283T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.585T= MANE Select ENSP00000261024.3:p.Ile195=
ENST00000261024.6:c.585T= ENSP00000261024.2:p.Ile195=
ENST00000427241.5:c.585T= ENSP00000390005.1:p.Ile195=
NM_014585.5:c.585T= , LRG_837t1:c.585T= NP_055400.1:p.Ile195=
XM_005246505.1:c.465T= XP_005246562.1:p.Ile155=
XM_005246505.2:c.465T= XP_005246562.1:p.Ile155=
XM_017003938.2:c.465T= XP_016859427.1:p.Ile155=
NM_014585.6:c.585T= MANE Select NP_055400.1:p.Ile195=