Canonical Allele Identifier: CA1675959494
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114960T= , CM000668.2:g.158114960T= GRCh38
NC_000006.11:g.158535992T= , CM000668.1:g.158535992T= GRCh37
NC_000006.10:g.158455980T= NCBI36
NG_032889.1:g.58321A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.725A= ENSP00000391168.2:n.725A=
ENST00000607071.6:c.*1233A= ENSP00000475855.1:n.*1233A=
ENST00000642244.1:c.1423A= ENSP00000493554.1:p.Lys475=
ENST00000642903.1:c.1513A= ENSP00000493559.1:p.Lys505=
ENST00000644972.1:c.1513A= ENSP00000496451.1:p.Lys505=
ENST00000645077.1:c.*1134A= ENSP00000496113.1:n.*1134A=
ENST00000645172.1:c.*1215A= ENSP00000495367.1:n.*1215A=
ENST00000646190.1:n.2844A=
ENST00000646208.1:c.1249A= ENSP00000493723.1:p.Lys417=
ENST00000646410.1:c.1384A= ENSP00000494205.1:p.Lys462=
ENST00000646562.1:c.*1347A= ENSP00000496087.1:n.*1347A=
ENST00000647468.2:c.1513A= MANE Select ENSP00000496731.1:p.Lys505=
ENST00000648111.1:c.*1201A= ENSP00000497275.1:n.*1201A=
ENST00000367101.5:c.1557A= ENSP00000356068.1:p.Ser519=
ENST00000367104.7:c.1513A= ENSP00000356071.3:p.Lys505=
ENST00000435180.5:c.238A= ENSP00000391168.1:p.Lys80=
ENST00000606965.5:c.*74A= ENSP00000475808.1:n.*74A=
ENST00000607071.5:c.*1447A= ENSP00000475855.1:n.*1447A=
ENST00000607742.5:c.*2791A= ENSP00000475523.1:n.*2791A=
NM_032861.3:c.1513A= NP_116250.3:p.Lys505=
NR_073096.1:n.1446A=
XM_006715586.1:c.1303A= XP_006715649.1:p.Lys435=
XM_011536196.1:c.1492A= XP_011534498.1:p.Lys498=
XM_011536197.1:c.1399A= XP_011534499.1:p.Lys467=
XM_011536198.1:c.1303A= XP_011534500.1:p.Lys435=
XM_006715586.3:c.1303A= XP_006715649.1:p.Lys435=
XM_011536196.3:c.1492A= XP_011534498.1:p.Lys498=
XM_011536198.3:c.1303A= XP_011534500.1:p.Lys435=
XM_024446573.1:c.1513A= XP_024302341.1:p.Lys505=
XR_001743697.2:n.1544A=
XR_942606.2:n.1595A=
NM_032861.4:c.1513A= MANE Select NP_116250.3:p.Lys505=
NR_073096.2:n.1428A=