Canonical Allele Identifier: CA1675959427
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114858A= , CM000668.2:g.158114858A= GRCh38
NC_000006.11:g.158535890A= , CM000668.1:g.158535890A= GRCh37
NC_000006.10:g.158455878A= NCBI36
NG_032889.1:g.58423T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.827T= ENSP00000391168.2:n.827T=
ENST00000607071.6:c.*1335T= ENSP00000475855.1:n.*1335T=
ENST00000642244.1:c.1525T= ENSP00000493554.1:p.Leu509=
ENST00000642903.1:c.1615T= ENSP00000493559.1:p.Leu539=
ENST00000644972.1:c.1615T= ENSP00000496451.1:p.Leu539=
ENST00000645077.1:c.*1236T= ENSP00000496113.1:n.*1236T=
ENST00000645172.1:c.*1317T= ENSP00000495367.1:n.*1317T=
ENST00000646190.1:n.2946T=
ENST00000646208.1:c.1351T= ENSP00000493723.1:p.Leu451=
ENST00000646410.1:c.1486T= ENSP00000494205.1:p.Leu496=
ENST00000646562.1:c.*1449T= ENSP00000496087.1:n.*1449T=
ENST00000647468.2:c.1615T= MANE Select ENSP00000496731.1:p.Leu539=
ENST00000648111.1:c.*1303T= ENSP00000497275.1:n.*1303T=
ENST00000367101.5:c.*63T= ENSP00000356068.1:n.*63T=
ENST00000367104.7:c.1615T= ENSP00000356071.3:p.Leu539=
ENST00000435180.5:c.340T= ENSP00000391168.1:p.Leu114=
ENST00000606965.5:c.*176T= ENSP00000475808.1:n.*176T=
ENST00000607071.5:c.*1549T= ENSP00000475855.1:n.*1549T=
ENST00000607742.5:c.*2893T= ENSP00000475523.1:n.*2893T=
NM_032861.3:c.1615T= NP_116250.3:p.Leu539=
NR_073096.1:n.1548T=
XM_006715586.1:c.1405T= XP_006715649.1:p.Leu469=
XM_011536196.1:c.1594T= XP_011534498.1:p.Leu532=
XM_011536197.1:c.1501T= XP_011534499.1:p.Leu501=
XM_011536198.1:c.1405T= XP_011534500.1:p.Leu469=
XM_006715586.3:c.1405T= XP_006715649.1:p.Leu469=
XM_011536196.3:c.1594T= XP_011534498.1:p.Leu532=
XM_011536198.3:c.1405T= XP_011534500.1:p.Leu469=
XM_024446573.1:c.1615T= XP_024302341.1:p.Leu539=
XR_001743697.2:n.1646T=
XR_942606.2:n.1697T=
NM_032861.4:c.1615T= MANE Select NP_116250.3:p.Leu539=
NR_073096.2:n.1530T=