Canonical Allele Identifier: CA366255168
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114921T>A , CM000668.2:g.158114921T>A GRCh38
NC_000006.11:g.158535953T>A , CM000668.1:g.158535953T>A GRCh37
NC_000006.10:g.158455941T>A NCBI36
NG_032889.1:g.58360A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.764A>T ENSP00000391168.2:n.764A>T
ENST00000607071.6:c.*1272A>T ENSP00000475855.1:n.*1272A>T
ENST00000642244.1:c.1462A>T ENSP00000493554.1:p.Ser488Cys
ENST00000642903.1:c.1552A>T ENSP00000493559.1:p.Ser518Cys
ENST00000644972.1:c.1552A>T ENSP00000496451.1:p.Ser518Cys
ENST00000645077.1:c.*1173A>T ENSP00000496113.1:n.*1173A>T
ENST00000645172.1:c.*1254A>T ENSP00000495367.1:n.*1254A>T
ENST00000646190.1:n.2883A>T
ENST00000646208.1:c.1288A>T ENSP00000493723.1:p.Ser430Cys
ENST00000646410.1:c.1423A>T ENSP00000494205.1:p.Ser475Cys
ENST00000646562.1:c.*1386A>T ENSP00000496087.1:n.*1386A>T
ENST00000647468.2:c.1552A>T MANE Select ENSP00000496731.1:p.Ser518Cys
ENST00000648111.1:c.*1240A>T ENSP00000497275.1:n.*1240A>T
ENST00000367101.5:c.1596A>T ENSP00000356068.1:p.Ter532Cys
ENST00000367104.7:c.1552A>T ENSP00000356071.3:p.Ser518Cys
ENST00000435180.5:c.277A>T ENSP00000391168.1:p.Ser93Cys
ENST00000606965.5:c.*113A>T ENSP00000475808.1:n.*113A>T
ENST00000607071.5:c.*1486A>T ENSP00000475855.1:n.*1486A>T
ENST00000607742.5:c.*2830A>T ENSP00000475523.1:n.*2830A>T
NM_032861.3:c.1552A>T NP_116250.3:p.Ser518Cys
NR_073096.1:n.1485A>T
XM_006715586.1:c.1342A>T XP_006715649.1:p.Ser448Cys
XM_011536196.1:c.1531A>T XP_011534498.1:p.Ser511Cys
XM_011536197.1:c.1438A>T XP_011534499.1:p.Ser480Cys
XM_011536198.1:c.1342A>T XP_011534500.1:p.Ser448Cys
XM_006715586.3:c.1342A>T XP_006715649.1:p.Ser448Cys
XM_011536196.3:c.1531A>T XP_011534498.1:p.Ser511Cys
XM_011536198.3:c.1342A>T XP_011534500.1:p.Ser448Cys
XM_024446573.1:c.1552A>T XP_024302341.1:p.Ser518Cys
XR_001743697.2:n.1583A>T
XR_942606.2:n.1634A>T
NM_032861.4:c.1552A>T MANE Select NP_116250.3:p.Ser518Cys
NR_073096.2:n.1467A>T