Canonical Allele Identifier: CA1335698084
Gene: SAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233346811_233346824delinsCAGGATGCAAATTT , CM000664.2:g.233346811_233346824delinsCAGGATGCAAATTT GRCh38
NC_000002.11:g.234255457_234255470delinsCAGGATGCAAATTT , CM000664.1:g.234255457_234255470delinsCAGGATGCAAATTT GRCh37
NC_000002.10:g.233920196_233920209delinsCAGGATGCAAATTT NCBI36
NG_009116.1:g.44149_44162delinsCAGGATGCAAATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000409110.6:c.1117_1130delinsCAGGATGCAAATTT MANE Select ENSP00000386444.1:p.Gln373=
ENST00000409110.5:c.1117_1130delinsCAGGATGCAAATTT ENSP00000386444.1:p.Gln373=
ENST00000412969.6:n.2337_2350delinsCAGGATGCAAATTT
ENST00000471884.5:n.3148_3161delinsCAGGATGCAAATTT
ENST00000474220.5:n.323_336delinsCAGGATGCAAATTT
ENST00000476500.5:n.6416_6429delinsCAGGATGCAAATTT
ENST00000492629.1:n.78_91delinsCAGGATGCAAATTT
NM_000541.4:c.1117_1130delinsCAGGATGCAAATTT NP_000532.2:p.Gln373=
XM_011511589.1:c.1117_1130delinsCAGGATGCAAATTT XP_011509891.1:p.Gln373=
XM_011511590.1:c.1117_1130delinsCAGGATGCAAATTT XP_011509892.1:p.Gln373=
XM_011511591.1:c.1107_1120delinsCAGGATGCAAATTT XP_011509893.1:p.Ile369=
XM_011511592.1:c.961_974delinsCAGGATGCAAATTT XP_011509894.1:p.Gln321=
XM_011511593.1:c.817_830delinsCAGGATGCAAATTT XP_011509895.1:p.Gln273=
XM_011511594.1:c.745_758delinsCAGGATGCAAATTT XP_011509896.1:p.Gln249=
XM_011511596.1:c.715_728delinsCAGGATGCAAATTT XP_011509898.1:p.Gln239=
XM_011511597.1:c.715_728delinsCAGGATGCAAATTT XP_011509899.1:p.Gln239=
XR_922978.1:n.1434_1447delinsCAGGATGCAAATTT
XR_922979.1:n.1438_1451delinsCAGGATGCAAATTT
XR_922980.1:n.1533_1546delinsCAGGATGCAAATTT
XM_011511593.3:c.817_830delinsCAGGATGCAAATTT XP_011509895.1:p.Gln273=
XM_017004641.1:c.1107_1120delinsCAGGATGCAAATTT XP_016860130.1:p.Ile369=
XM_024453036.1:c.705_718delinsCAGGATGCAAATTT XP_024308804.1:p.Ile235=
XR_001738882.1:n.1315_1328delinsCAGGATGCAAATTT
XR_922980.2:n.1533_1546delinsCAGGATGCAAATTT
NM_000541.5:c.1117_1130delinsCAGGATGCAAATTT MANE Select NP_000532.2:p.Gln373=