Canonical Allele Identifier: CA1676923390
Gene: SLC22A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160139408_160139410delinsGTC , CM000668.2:g.160139408_160139410delinsGTC GRCh38
NC_000006.11:g.160560440_160560442delinsGTC , CM000668.1:g.160560440_160560442delinsGTC GRCh37
NC_000006.10:g.160480430_160480432delinsGTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366963.9:c.1062-245_1062-243delinsGTC MANE Select ENSP00000355930.4:n.1062-245_1062-243delinsGTC
ENST00000324965.8:c.1062-245_1062-243delinsGTC ENSP00000318103.4:n.1062-245_1062-243delinsGTC
ENST00000366963.8:c.1062-245_1062-243delinsGTC ENSP00000355930.4:n.1062-245_1062-243delinsGTC
ENST00000457470.6:c.1062-245_1062-243delinsGTC ENSP00000409557.2:n.1062-245_1062-243delinsGTC
ENST00000460902.2:c.1061+2758_1061+2760delinsGTC ENSP00000439274.1:n.1061+2758_1061+2760delinsGTC
ENST00000539263.5:c.*535-245_*535-243delinsGTC ENSP00000443245.1:n.*535-245_*535-243delinsGTC
NM_003057.2:c.1062-245_1062-243delinsGTC NP_003048.1:n.1062-245_1062-243delinsGTC
NM_153187.1:c.1062-245_1062-243delinsGTC NP_694857.1:n.1062-245_1062-243delinsGTC
XM_005267102.3:c.1062-245_1062-243delinsGTC XP_005267159.1:n.1062-245_1062-243delinsGTC
XM_005267103.1:c.1062-245_1062-243delinsGTC XP_005267160.1:n.1062-245_1062-243delinsGTC
XM_005267104.3:c.486-245_486-243delinsGTC XP_005267161.1:n.486-245_486-243delinsGTC
XM_005267105.3:c.486-245_486-243delinsGTC XP_005267162.1:n.486-245_486-243delinsGTC
XM_006715552.1:c.1062-245_1062-243delinsGTC XP_006715615.1:n.1062-245_1062-243delinsGTC
XM_011536074.1:c.486-245_486-243delinsGTC XP_011534376.1:n.486-245_486-243delinsGTC
XM_005267102.5:c.1062-245_1062-243delinsGTC XP_005267159.1:n.1062-245_1062-243delinsGTC
XM_005267103.2:c.1062-245_1062-243delinsGTC XP_005267160.1:n.1062-245_1062-243delinsGTC
XM_005267104.5:c.486-245_486-243delinsGTC XP_005267161.1:n.486-245_486-243delinsGTC
XM_005267105.5:c.486-245_486-243delinsGTC XP_005267162.1:n.486-245_486-243delinsGTC
XM_006715552.2:c.1062-245_1062-243delinsGTC XP_006715615.1:n.1062-245_1062-243delinsGTC
XM_011536074.3:c.486-245_486-243delinsGTC XP_011534376.1:n.486-245_486-243delinsGTC
NM_003057.3:c.1062-245_1062-243delinsGTC MANE Select NP_003048.1:n.1062-245_1062-243delinsGTC
NM_153187.2:c.1062-245_1062-243delinsGTC NP_694857.1:n.1062-245_1062-243delinsGTC