Canonical Allele Identifier: CA1676930186
Gene: SLC22A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160154815T= , CM000668.2:g.160154815T= GRCh38
NC_000006.11:g.160575847T= , CM000668.1:g.160575847T= GRCh37
NC_000006.10:g.160495837T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366963.9:c.1403T= MANE Select ENSP00000355930.4:p.Val468=
ENST00000324965.8:c.1386-1160T= ENSP00000318103.4:n.1386-1160T=
ENST00000366963.8:c.1403T= ENSP00000355930.4:p.Val468=
ENST00000457470.6:c.1386-3701T= ENSP00000409557.2:n.1386-3701T=
ENST00000460902.2:c.1188T= ENSP00000439274.1:n.1188T=
ENST00000539263.5:c.*876T= ENSP00000443245.1:n.*876T=
NM_003057.2:c.1403T= NP_003048.1:p.Val468=
NM_153187.1:c.1386-1160T= NP_694857.1:n.1386-1160T=
XM_005267102.3:c.1403T= XP_005267159.1:p.Val468=
XM_005267103.1:c.1403T= XP_005267160.1:p.Val468=
XM_005267104.3:c.827T= XP_005267161.1:p.Val276=
XM_005267105.3:c.827T= XP_005267162.1:p.Val276=
XM_006715552.1:c.1386-3701T= XP_006715615.1:n.1386-3701T=
XM_011536074.1:c.827T= XP_011534376.1:p.Val276=
XM_005267102.5:c.1403T= XP_005267159.1:p.Val468=
XM_005267103.2:c.1403T= XP_005267160.1:p.Val468=
XM_005267104.5:c.827T= XP_005267161.1:p.Val276=
XM_005267105.5:c.827T= XP_005267162.1:p.Val276=
XM_006715552.2:c.1386-3701T= XP_006715615.1:n.1386-3701T=
XM_011536074.3:c.827T= XP_011534376.1:p.Val276=
NM_003057.3:c.1403T= MANE Select NP_003048.1:p.Val468=
NM_153187.2:c.1386-1160T= NP_694857.1:n.1386-1160T=