Canonical Allele Identifier: CA2701181547
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs2105620638

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564232_189564233insATTCAGCTGTTTCAATTCA , CM000664.2:g.189564232_189564233insATTCAGCTGTTTCAATTCA GRCh38
NC_000002.11:g.190428958_190428959insATTCAGCTGTTTCAATTCA , CM000664.1:g.190428958_190428959insATTCAGCTGTTTCAATTCA GRCh37
NC_000002.10:g.190137203_190137204insATTCAGCTGTTTCAATTCA NCBI36
NG_009027.1:g.21580_21581insGAATTGAAACAGCTGAATT , LRG_837:g.21580_21581insGAATTGAAACAGCTGAATT

Transcript Alleles

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