Canonical Allele Identifier: CA1675959440
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114873G= , CM000668.2:g.158114873G= GRCh38
NC_000006.11:g.158535905G= , CM000668.1:g.158535905G= GRCh37
NC_000006.10:g.158455893G= NCBI36
NG_032889.1:g.58408C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.812C= ENSP00000391168.2:n.812C=
ENST00000607071.6:c.*1320C= ENSP00000475855.1:n.*1320C=
ENST00000642244.1:c.1510C= ENSP00000493554.1:p.His504=
ENST00000642903.1:c.1600C= ENSP00000493559.1:p.His534=
ENST00000644972.1:c.1600C= ENSP00000496451.1:p.His534=
ENST00000645077.1:c.*1221C= ENSP00000496113.1:n.*1221C=
ENST00000645172.1:c.*1302C= ENSP00000495367.1:n.*1302C=
ENST00000646190.1:n.2931C=
ENST00000646208.1:c.1336C= ENSP00000493723.1:p.His446=
ENST00000646410.1:c.1471C= ENSP00000494205.1:p.His491=
ENST00000646562.1:c.*1434C= ENSP00000496087.1:n.*1434C=
ENST00000647468.2:c.1600C= MANE Select ENSP00000496731.1:p.His534=
ENST00000648111.1:c.*1288C= ENSP00000497275.1:n.*1288C=
ENST00000367101.5:c.*48C= ENSP00000356068.1:n.*48C=
ENST00000367104.7:c.1600C= ENSP00000356071.3:p.His534=
ENST00000435180.5:c.325C= ENSP00000391168.1:p.His109=
ENST00000606965.5:c.*161C= ENSP00000475808.1:n.*161C=
ENST00000607071.5:c.*1534C= ENSP00000475855.1:n.*1534C=
ENST00000607742.5:c.*2878C= ENSP00000475523.1:n.*2878C=
NM_032861.3:c.1600C= NP_116250.3:p.His534=
NR_073096.1:n.1533C=
XM_006715586.1:c.1390C= XP_006715649.1:p.His464=
XM_011536196.1:c.1579C= XP_011534498.1:p.His527=
XM_011536197.1:c.1486C= XP_011534499.1:p.His496=
XM_011536198.1:c.1390C= XP_011534500.1:p.His464=
XM_006715586.3:c.1390C= XP_006715649.1:p.His464=
XM_011536196.3:c.1579C= XP_011534498.1:p.His527=
XM_011536198.3:c.1390C= XP_011534500.1:p.His464=
XM_024446573.1:c.1600C= XP_024302341.1:p.His534=
XR_001743697.2:n.1631C=
XR_942606.2:n.1682C=
NM_032861.4:c.1600C= MANE Select NP_116250.3:p.His534=
NR_073096.2:n.1515C=