Canonical Allele Identifier: CA1675959495
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114962A= , CM000668.2:g.158114962A= GRCh38
NC_000006.11:g.158535994A= , CM000668.1:g.158535994A= GRCh37
NC_000006.10:g.158455982A= NCBI36
NG_032889.1:g.58319T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.723T= ENSP00000391168.2:n.723T=
ENST00000607071.6:c.*1231T= ENSP00000475855.1:n.*1231T=
ENST00000642244.1:c.1421T= ENSP00000493554.1:p.Val474=
ENST00000642903.1:c.1511T= ENSP00000493559.1:p.Val504=
ENST00000644972.1:c.1511T= ENSP00000496451.1:p.Val504=
ENST00000645077.1:c.*1132T= ENSP00000496113.1:n.*1132T=
ENST00000645172.1:c.*1213T= ENSP00000495367.1:n.*1213T=
ENST00000646190.1:n.2842T=
ENST00000646208.1:c.1247T= ENSP00000493723.1:p.Val416=
ENST00000646410.1:c.1382T= ENSP00000494205.1:p.Val461=
ENST00000646562.1:c.*1345T= ENSP00000496087.1:n.*1345T=
ENST00000647468.2:c.1511T= MANE Select ENSP00000496731.1:p.Val504=
ENST00000648111.1:c.*1199T= ENSP00000497275.1:n.*1199T=
ENST00000367101.5:c.1555T= ENSP00000356068.1:p.Ser519=
ENST00000367104.7:c.1511T= ENSP00000356071.3:p.Val504=
ENST00000435180.5:c.236T= ENSP00000391168.1:p.Val79=
ENST00000606965.5:c.*72T= ENSP00000475808.1:n.*72T=
ENST00000607071.5:c.*1445T= ENSP00000475855.1:n.*1445T=
ENST00000607742.5:c.*2789T= ENSP00000475523.1:n.*2789T=
NM_032861.3:c.1511T= NP_116250.3:p.Val504=
NR_073096.1:n.1444T=
XM_006715586.1:c.1301T= XP_006715649.1:p.Val434=
XM_011536196.1:c.1490T= XP_011534498.1:p.Val497=
XM_011536197.1:c.1397T= XP_011534499.1:p.Val466=
XM_011536198.1:c.1301T= XP_011534500.1:p.Val434=
XM_006715586.3:c.1301T= XP_006715649.1:p.Val434=
XM_011536196.3:c.1490T= XP_011534498.1:p.Val497=
XM_011536198.3:c.1301T= XP_011534500.1:p.Val434=
XM_024446573.1:c.1511T= XP_024302341.1:p.Val504=
XR_001743697.2:n.1542T=
XR_942606.2:n.1593T=
NM_032861.4:c.1511T= MANE Select NP_116250.3:p.Val504=
NR_073096.2:n.1426T=