Canonical Allele Identifier: CA2701181397
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs2105620629

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564227_189564228insTT , CM000664.2:g.189564227_189564228insTT GRCh38
NC_000002.11:g.190428953_190428954insTT , CM000664.1:g.190428953_190428954insTT GRCh37
NC_000002.10:g.190137198_190137199insTT NCBI36
NG_009027.1:g.21585_21586insAA , LRG_837:g.21585_21586insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.761-2_761-1insAA MANE Select ENSP00000261024.3:n.761-2_761-1insAA
ENST00000261024.6:c.761-2_761-1insAA ENSP00000261024.2:n.761-2_761-1insAA
NM_014585.5:c.761-2_761-1insAA , LRG_837t1:c.761-2_761-1insAA NP_055400.1:n.761-2_761-1insAA
XM_005246505.1:c.641-2_641-1insAA XP_005246562.1:n.641-2_641-1insAA
XM_005246505.2:c.641-2_641-1insAA XP_005246562.1:n.641-2_641-1insAA
XM_017003938.2:c.641-2_641-1insAA XP_016859427.1:n.641-2_641-1insAA
NM_014585.6:c.761-2_761-1insAA MANE Select NP_055400.1:n.761-2_761-1insAA