Canonical Allele Identifier: CA2681066214
Gene: SLC22A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160154990_160154991insCAC , CM000668.2:g.160154990_160154991insCAC GRCh38
NC_000006.11:g.160576022_160576023insCAC , CM000668.1:g.160576022_160576023insCAC GRCh37
NC_000006.10:g.160496012_160496013insCAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366963.9:c.1498+80_1498+81insCAC MANE Select ENSP00000355930.4:n.1498+80_1498+81insCAC
ENST00000324965.8:c.1386-985_1386-984insCAC ENSP00000318103.4:n.1386-985_1386-984insCAC
ENST00000366963.8:c.1498+80_1498+81insCAC ENSP00000355930.4:n.1498+80_1498+81insCAC
ENST00000457470.6:c.1386-3526_1386-3525insCAC ENSP00000409557.2:n.1386-3526_1386-3525insCAC
ENST00000460902.2:c.1283+80_1283+81insCAC ENSP00000439274.1:n.1283+80_1283+81insCAC
ENST00000539263.5:c.*971+80_*971+81insCAC ENSP00000443245.1:n.*971+80_*971+81insCAC
NM_003057.2:c.1498+80_1498+81insCAC NP_003048.1:n.1498+80_1498+81insCAC
NM_153187.1:c.1386-985_1386-984insCAC NP_694857.1:n.1386-985_1386-984insCAC
XM_005267102.3:c.1498+80_1498+81insCAC XP_005267159.1:n.1498+80_1498+81insCAC
XM_005267103.1:c.1498+80_1498+81insCAC XP_005267160.1:n.1498+80_1498+81insCAC
XM_005267104.3:c.922+80_922+81insCAC XP_005267161.1:n.922+80_922+81insCAC
XM_005267105.3:c.922+80_922+81insCAC XP_005267162.1:n.922+80_922+81insCAC
XM_006715552.1:c.1386-3526_1386-3525insCAC XP_006715615.1:n.1386-3526_1386-3525insCAC
XM_011536074.1:c.922+80_922+81insCAC XP_011534376.1:n.922+80_922+81insCAC
XM_005267102.5:c.1498+80_1498+81insCAC XP_005267159.1:n.1498+80_1498+81insCAC
XM_005267103.2:c.1498+80_1498+81insCAC XP_005267160.1:n.1498+80_1498+81insCAC
XM_005267104.5:c.922+80_922+81insCAC XP_005267161.1:n.922+80_922+81insCAC
XM_005267105.5:c.922+80_922+81insCAC XP_005267162.1:n.922+80_922+81insCAC
XM_006715552.2:c.1386-3526_1386-3525insCAC XP_006715615.1:n.1386-3526_1386-3525insCAC
XM_011536074.3:c.922+80_922+81insCAC XP_011534376.1:n.922+80_922+81insCAC
NM_003057.3:c.1498+80_1498+81insCAC MANE Select NP_003048.1:n.1498+80_1498+81insCAC
NM_153187.2:c.1386-985_1386-984insCAC NP_694857.1:n.1386-985_1386-984insCAC