Canonical Allele Identifier: CA1676930268
Gene: SLC22A1 HGNC NCBI

Linked Data

dbSNP Id: rs1781607941

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160154984_160154985insACTCA , CM000668.2:g.160154984_160154985insACTCA GRCh38
NC_000006.11:g.160576016_160576017insACTCA , CM000668.1:g.160576016_160576017insACTCA GRCh37
NC_000006.10:g.160496006_160496007insACTCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366963.9:c.1498+74_1498+75insACTCA MANE Select ENSP00000355930.4:n.1498+74_1498+75insACTCA
ENST00000324965.8:c.1386-991_1386-990insACTCA ENSP00000318103.4:n.1386-991_1386-990insACTCA
ENST00000366963.8:c.1498+74_1498+75insACTCA ENSP00000355930.4:n.1498+74_1498+75insACTCA
ENST00000457470.6:c.1386-3532_1386-3531insACTCA ENSP00000409557.2:n.1386-3532_1386-3531insACTCA
ENST00000460902.2:c.1283+74_1283+75insACTCA ENSP00000439274.1:n.1283+74_1283+75insACTCA
ENST00000539263.5:c.*971+74_*971+75insACTCA ENSP00000443245.1:n.*971+74_*971+75insACTCA
NM_003057.2:c.1498+74_1498+75insACTCA NP_003048.1:n.1498+74_1498+75insACTCA
NM_153187.1:c.1386-991_1386-990insACTCA NP_694857.1:n.1386-991_1386-990insACTCA
XM_005267102.3:c.1498+74_1498+75insACTCA XP_005267159.1:n.1498+74_1498+75insACTCA
XM_005267103.1:c.1498+74_1498+75insACTCA XP_005267160.1:n.1498+74_1498+75insACTCA
XM_005267104.3:c.922+74_922+75insACTCA XP_005267161.1:n.922+74_922+75insACTCA
XM_005267105.3:c.922+74_922+75insACTCA XP_005267162.1:n.922+74_922+75insACTCA
XM_006715552.1:c.1386-3532_1386-3531insACTCA XP_006715615.1:n.1386-3532_1386-3531insACTCA
XM_011536074.1:c.922+74_922+75insACTCA XP_011534376.1:n.922+74_922+75insACTCA
XM_005267102.5:c.1498+74_1498+75insACTCA XP_005267159.1:n.1498+74_1498+75insACTCA
XM_005267103.2:c.1498+74_1498+75insACTCA XP_005267160.1:n.1498+74_1498+75insACTCA
XM_005267104.5:c.922+74_922+75insACTCA XP_005267161.1:n.922+74_922+75insACTCA
XM_005267105.5:c.922+74_922+75insACTCA XP_005267162.1:n.922+74_922+75insACTCA
XM_006715552.2:c.1386-3532_1386-3531insACTCA XP_006715615.1:n.1386-3532_1386-3531insACTCA
XM_011536074.3:c.922+74_922+75insACTCA XP_011534376.1:n.922+74_922+75insACTCA
NM_003057.3:c.1498+74_1498+75insACTCA MANE Select NP_003048.1:n.1498+74_1498+75insACTCA
NM_153187.2:c.1386-991_1386-990insACTCA NP_694857.1:n.1386-991_1386-990insACTCA