Canonical Allele Identifier: CA1675959468
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114911A= , CM000668.2:g.158114911A= GRCh38
NC_000006.11:g.158535943A= , CM000668.1:g.158535943A= GRCh37
NC_000006.10:g.158455931A= NCBI36
NG_032889.1:g.58370T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.774T= ENSP00000391168.2:n.774T=
ENST00000607071.6:c.*1282T= ENSP00000475855.1:n.*1282T=
ENST00000642244.1:c.1472T= ENSP00000493554.1:p.Ile491=
ENST00000642903.1:c.1562T= ENSP00000493559.1:p.Ile521=
ENST00000644972.1:c.1562T= ENSP00000496451.1:p.Ile521=
ENST00000645077.1:c.*1183T= ENSP00000496113.1:n.*1183T=
ENST00000645172.1:c.*1264T= ENSP00000495367.1:n.*1264T=
ENST00000646190.1:n.2893T=
ENST00000646208.1:c.1298T= ENSP00000493723.1:p.Ile433=
ENST00000646410.1:c.1433T= ENSP00000494205.1:p.Ile478=
ENST00000646562.1:c.*1396T= ENSP00000496087.1:n.*1396T=
ENST00000647468.2:c.1562T= MANE Select ENSP00000496731.1:p.Ile521=
ENST00000648111.1:c.*1250T= ENSP00000497275.1:n.*1250T=
ENST00000367101.5:c.*10T= ENSP00000356068.1:n.*10T=
ENST00000367104.7:c.1562T= ENSP00000356071.3:p.Ile521=
ENST00000435180.5:c.287T= ENSP00000391168.1:p.Ile96=
ENST00000606965.5:c.*123T= ENSP00000475808.1:n.*123T=
ENST00000607071.5:c.*1496T= ENSP00000475855.1:n.*1496T=
ENST00000607742.5:c.*2840T= ENSP00000475523.1:n.*2840T=
NM_032861.3:c.1562T= NP_116250.3:p.Ile521=
NR_073096.1:n.1495T=
XM_006715586.1:c.1352T= XP_006715649.1:p.Ile451=
XM_011536196.1:c.1541T= XP_011534498.1:p.Ile514=
XM_011536197.1:c.1448T= XP_011534499.1:p.Ile483=
XM_011536198.1:c.1352T= XP_011534500.1:p.Ile451=
XM_006715586.3:c.1352T= XP_006715649.1:p.Ile451=
XM_011536196.3:c.1541T= XP_011534498.1:p.Ile514=
XM_011536198.3:c.1352T= XP_011534500.1:p.Ile451=
XM_024446573.1:c.1562T= XP_024302341.1:p.Ile521=
XR_001743697.2:n.1593T=
XR_942606.2:n.1644T=
NM_032861.4:c.1562T= MANE Select NP_116250.3:p.Ile521=
NR_073096.2:n.1477T=