Canonical Allele Identifier: CA2681066175
Gene: SLC22A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160154942_160154943insACTCAACAAATACGACTGAGTACTCACAC , CM000668.2:g.160154942_160154943insACTCAACAAATACGACTGAGTACTCACAC GRCh38
NC_000006.11:g.160575974_160575975insACTCAACAAATACGACTGAGTACTCACAC , CM000668.1:g.160575974_160575975insACTCAACAAATACGACTGAGTACTCACAC GRCh37
NC_000006.10:g.160495964_160495965insACTCAACAAATACGACTGAGTACTCACAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366963.9:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC MANE Select ENSP00000355930.4:n.1498+32_1498+33insACTCAACAAATACGACTGAGTAC...
ENST00000324965.8:c.1386-1033_1386-1032insACTCAACAAATACGACTGAGTACTCACAC ENSP00000318103.4:n.1386-1033_1386-1032insACTCAACAAATACGACTGA...
ENST00000366963.8:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC ENSP00000355930.4:n.1498+32_1498+33insACTCAACAAATACGACTGAGTAC...
ENST00000457470.6:c.1386-3574_1386-3573insACTCAACAAATACGACTGAGTACTCACAC ENSP00000409557.2:n.1386-3574_1386-3573insACTCAACAAATACGACTGA...
ENST00000460902.2:c.1283+32_1283+33insACTCAACAAATACGACTGAGTACTCACAC ENSP00000439274.1:n.1283+32_1283+33insACTCAACAAATACGACTGAGTAC...
ENST00000539263.5:c.*971+32_*971+33insACTCAACAAATACGACTGAGTACTCACAC ENSP00000443245.1:n.*971+32_*971+33insACTCAACAAATACGACTGAGTAC...
NM_003057.2:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC NP_003048.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC...
NM_153187.1:c.1386-1033_1386-1032insACTCAACAAATACGACTGAGTACTCACAC NP_694857.1:n.1386-1033_1386-1032insACTCAACAAATACGACTGAGTACTC...
XM_005267102.3:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267159.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCA...
XM_005267103.1:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267160.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCA...
XM_005267104.3:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267161.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
XM_005267105.3:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267162.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
XM_006715552.1:c.1386-3574_1386-3573insACTCAACAAATACGACTGAGTACTCACAC XP_006715615.1:n.1386-3574_1386-3573insACTCAACAAATACGACTGAGTA...
XM_011536074.1:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_011534376.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
XM_005267102.5:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267159.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCA...
XM_005267103.2:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267160.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCA...
XM_005267104.5:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267161.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
XM_005267105.5:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_005267162.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
XM_006715552.2:c.1386-3574_1386-3573insACTCAACAAATACGACTGAGTACTCACAC XP_006715615.1:n.1386-3574_1386-3573insACTCAACAAATACGACTGAGTA...
XM_011536074.3:c.922+32_922+33insACTCAACAAATACGACTGAGTACTCACAC XP_011534376.1:n.922+32_922+33insACTCAACAAATACGACTGAGTACTCACA...
NM_003057.3:c.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC MANE Select NP_003048.1:n.1498+32_1498+33insACTCAACAAATACGACTGAGTACTCACAC...
NM_153187.2:c.1386-1033_1386-1032insACTCAACAAATACGACTGAGTACTCACAC NP_694857.1:n.1386-1033_1386-1032insACTCAACAAATACGACTGAGTACTC...