Canonical Allele Identifier: CA151158389
Gene: SLC22A1 HGNC NCBI

Linked Data

dbSNP Id: rs35191146
MyVariant Identifiers: chr6:g.160560883del (hg19) chr6:g.160139851del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160139851del , CM000668.2:g.160139851del GRCh38
NC_000006.11:g.160560883del , CM000668.1:g.160560883del GRCh37
NC_000006.10:g.160480873del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366963.9:c.1260del MANE Select ENSP00000355930.4:p.Met420IlefsTer11
ENST00000324965.8:c.1260del ENSP00000318103.4:p.Met420IlefsTer11
ENST00000366963.8:c.1260del ENSP00000355930.4:p.Met420IlefsTer11
ENST00000457470.6:c.1260del ENSP00000409557.2:p.Met420IlefsTer11
ENST00000460902.2:c.1061+3201del ENSP00000439274.1:n.1061+3201del
ENST00000539263.5:c.*733del ENSP00000443245.1:n.*733del
NM_003057.2:c.1260del NP_003048.1:p.Met420IlefsTer11
NM_153187.1:c.1260del NP_694857.1:p.Met420IlefsTer11
XM_005267102.3:c.1260del XP_005267159.1:p.Met420IlefsTer11
XM_005267103.1:c.1260del XP_005267160.1:p.Met420IlefsTer11
XM_005267104.3:c.684del XP_005267161.1:p.Met228IlefsTer11
XM_005267105.3:c.684del XP_005267162.1:p.Met228IlefsTer11
XM_006715552.1:c.1260del XP_006715615.1:p.Met420IlefsTer11
XM_011536074.1:c.684del XP_011534376.1:p.Met228IlefsTer11
XM_005267102.5:c.1260del XP_005267159.1:p.Met420IlefsTer11
XM_005267103.2:c.1260del XP_005267160.1:p.Met420IlefsTer11
XM_005267104.5:c.684del XP_005267161.1:p.Met228IlefsTer11
XM_005267105.5:c.684del XP_005267162.1:p.Met228IlefsTer11
XM_006715552.2:c.1260del XP_006715615.1:p.Met420IlefsTer11
XM_011536074.3:c.684del XP_011534376.1:p.Met228IlefsTer11
NM_003057.3:c.1260del MANE Select NP_003048.1:p.Met420IlefsTer11
NM_153187.2:c.1260del NP_694857.1:p.Met420IlefsTer11
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