Canonical Allele Identifier: CA1675959421
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114852C= , CM000668.2:g.158114852C= GRCh38
NC_000006.11:g.158535884C= , CM000668.1:g.158535884C= GRCh37
NC_000006.10:g.158455872C= NCBI36
NG_032889.1:g.58429G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.833G= ENSP00000391168.2:n.833G=
ENST00000607071.6:c.*1341G= ENSP00000475855.1:n.*1341G=
ENST00000642244.1:c.1531G= ENSP00000493554.1:p.Glu511=
ENST00000642903.1:c.1621G= ENSP00000493559.1:p.Glu541=
ENST00000644972.1:c.1621G= ENSP00000496451.1:p.Glu541=
ENST00000645077.1:c.*1242G= ENSP00000496113.1:n.*1242G=
ENST00000645172.1:c.*1323G= ENSP00000495367.1:n.*1323G=
ENST00000646190.1:n.2952G=
ENST00000646208.1:c.1357G= ENSP00000493723.1:p.Glu453=
ENST00000646410.1:c.1492G= ENSP00000494205.1:p.Glu498=
ENST00000646562.1:c.*1455G= ENSP00000496087.1:n.*1455G=
ENST00000647468.2:c.1621G= MANE Select ENSP00000496731.1:p.Glu541=
ENST00000648111.1:c.*1309G= ENSP00000497275.1:n.*1309G=
ENST00000367101.5:c.*69G= ENSP00000356068.1:n.*69G=
ENST00000367104.7:c.1621G= ENSP00000356071.3:p.Glu541=
ENST00000435180.5:c.346G= ENSP00000391168.1:p.Glu116=
ENST00000606965.5:c.*182G= ENSP00000475808.1:n.*182G=
ENST00000607071.5:c.*1555G= ENSP00000475855.1:n.*1555G=
ENST00000607742.5:c.*2899G= ENSP00000475523.1:n.*2899G=
NM_032861.3:c.1621G= NP_116250.3:p.Glu541=
NR_073096.1:n.1554G=
XM_006715586.1:c.1411G= XP_006715649.1:p.Glu471=
XM_011536196.1:c.1600G= XP_011534498.1:p.Glu534=
XM_011536197.1:c.1507G= XP_011534499.1:p.Glu503=
XM_011536198.1:c.1411G= XP_011534500.1:p.Glu471=
XM_006715586.3:c.1411G= XP_006715649.1:p.Glu471=
XM_011536196.3:c.1600G= XP_011534498.1:p.Glu534=
XM_011536198.3:c.1411G= XP_011534500.1:p.Glu471=
XM_024446573.1:c.1621G= XP_024302341.1:p.Glu541=
XR_001743697.2:n.1652G=
XR_942606.2:n.1703G=
NM_032861.4:c.1621G= MANE Select NP_116250.3:p.Glu541=
NR_073096.2:n.1536G=