Canonical Allele Identifier: CA366255286
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114964A>C , CM000668.2:g.158114964A>C GRCh38
NC_000006.11:g.158535996A>C , CM000668.1:g.158535996A>C GRCh37
NC_000006.10:g.158455984A>C NCBI36
NG_032889.1:g.58317T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.721T>G ENSP00000391168.2:n.721T>G
ENST00000607071.6:c.*1229T>G ENSP00000475855.1:n.*1229T>G
ENST00000642244.1:c.1419T>G ENSP00000493554.1:p.Leu473=
ENST00000642903.1:c.1509T>G ENSP00000493559.1:p.Leu503=
ENST00000644972.1:c.1509T>G ENSP00000496451.1:p.Leu503=
ENST00000645077.1:c.*1130T>G ENSP00000496113.1:n.*1130T>G
ENST00000645172.1:c.*1211T>G ENSP00000495367.1:n.*1211T>G
ENST00000646190.1:n.2840T>G
ENST00000646208.1:c.1245T>G ENSP00000493723.1:p.Leu415=
ENST00000646410.1:c.1380T>G ENSP00000494205.1:p.Leu460=
ENST00000646562.1:c.*1343T>G ENSP00000496087.1:n.*1343T>G
ENST00000647468.2:c.1509T>G MANE Select ENSP00000496731.1:p.Leu503=
ENST00000648111.1:c.*1197T>G ENSP00000497275.1:n.*1197T>G
ENST00000367101.5:c.1553T>G ENSP00000356068.1:p.Leu518Trp
ENST00000367104.7:c.1509T>G ENSP00000356071.3:p.Leu503=
ENST00000435180.5:c.234T>G ENSP00000391168.1:p.Leu78=
ENST00000606965.5:c.*70T>G ENSP00000475808.1:n.*70T>G
ENST00000607071.5:c.*1443T>G ENSP00000475855.1:n.*1443T>G
ENST00000607742.5:c.*2787T>G ENSP00000475523.1:n.*2787T>G
NM_032861.3:c.1509T>G NP_116250.3:p.Leu503=
NR_073096.1:n.1442T>G
XM_006715586.1:c.1299T>G XP_006715649.1:p.Leu433=
XM_011536196.1:c.1488T>G XP_011534498.1:p.Leu496=
XM_011536197.1:c.1395T>G XP_011534499.1:p.Leu465=
XM_011536198.1:c.1299T>G XP_011534500.1:p.Leu433=
XM_006715586.3:c.1299T>G XP_006715649.1:p.Leu433=
XM_011536196.3:c.1488T>G XP_011534498.1:p.Leu496=
XM_011536198.3:c.1299T>G XP_011534500.1:p.Leu433=
XM_024446573.1:c.1509T>G XP_024302341.1:p.Leu503=
XR_001743697.2:n.1540T>G
XR_942606.2:n.1591T>G
NM_032861.4:c.1509T>G MANE Select NP_116250.3:p.Leu503=
NR_073096.2:n.1424T>G