Canonical Allele Identifier: CA1676920001
Gene: SLC22A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160132198C= , CM000668.2:g.160132198C= GRCh38
NC_000006.11:g.160553230C= , CM000668.1:g.160553230C= GRCh37
NC_000006.10:g.160473220C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366963.9:c.516-34C= MANE Select ENSP00000355930.4:n.516-34C=
ENST00000324965.8:c.516-34C= ENSP00000318103.4:n.516-34C=
ENST00000366963.8:c.516-34C= ENSP00000355930.4:n.516-34C=
ENST00000457470.6:c.516-34C= ENSP00000409557.2:n.516-34C=
ENST00000460902.2:c.516-34C= ENSP00000439274.1:n.516-34C=
ENST00000539263.5:c.412-34C= ENSP00000443245.1:n.412-34C=
ENST00000540443.1:c.-61-34C= ENSP00000440105.1:n.-61-34C=
NM_003057.2:c.516-34C= NP_003048.1:n.516-34C=
NM_153187.1:c.516-34C= NP_694857.1:n.516-34C=
XM_005267102.3:c.516-34C= XP_005267159.1:n.516-34C=
XM_005267103.1:c.516-34C= XP_005267160.1:n.516-34C=
XM_005267104.3:c.-61-34C= XP_005267161.1:n.-61-34C=
XM_005267105.3:c.-61-34C= XP_005267162.1:n.-61-34C=
XM_006715552.1:c.516-34C= XP_006715615.1:n.516-34C=
XM_011536074.1:c.-61-34C= XP_011534376.1:n.-61-34C=
XM_005267102.5:c.516-34C= XP_005267159.1:n.516-34C=
XM_005267103.2:c.516-34C= XP_005267160.1:n.516-34C=
XM_005267104.5:c.-61-34C= XP_005267161.1:n.-61-34C=
XM_005267105.5:c.-61-34C= XP_005267162.1:n.-61-34C=
XM_006715552.2:c.516-34C= XP_006715615.1:n.516-34C=
XM_011536074.3:c.-61-34C= XP_011534376.1:n.-61-34C=
NM_003057.3:c.516-34C= MANE Select NP_003048.1:n.516-34C=
NM_153187.2:c.516-34C= NP_694857.1:n.516-34C=