Canonical Allele Identifier: CA2577188078
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563536dup , CM000664.2:g.189563536dup GRCh38
NC_000002.11:g.190428262dup , CM000664.1:g.190428262dup GRCh37
NC_000002.10:g.190136507dup NCBI36
NG_009027.1:g.22277dup , LRG_837:g.22277dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+49dup MANE Select ENSP00000261024.3:n.1402+49dup
ENST00000261024.6:c.1402+49dup ENSP00000261024.2:n.1402+49dup
NM_014585.5:c.1402+49dup , LRG_837t1:c.1402+49dup NP_055400.1:n.1402+49dup
XM_005246505.1:c.1282+49dup XP_005246562.1:n.1282+49dup
XM_005246505.2:c.1282+49dup XP_005246562.1:n.1282+49dup
XM_017003938.2:c.1282+49dup XP_016859427.1:n.1282+49dup
NM_014585.6:c.1402+49dup MANE Select NP_055400.1:n.1402+49dup