Canonical Allele Identifier: CA1675959339
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114803T= , CM000668.2:g.158114803T= GRCh38
NC_000006.11:g.158535835T= , CM000668.1:g.158535835T= GRCh37
NC_000006.10:g.158455823T= NCBI36
NG_032889.1:g.58478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1390A= ENSP00000475855.1:n.*1390A=
ENST00000642244.1:c.1580A= ENSP00000493554.1:p.Lys527=
ENST00000642903.1:c.1670A= ENSP00000493559.1:p.Lys557=
ENST00000644972.1:c.1670A= ENSP00000496451.1:p.Lys557=
ENST00000645077.1:c.*1291A= ENSP00000496113.1:n.*1291A=
ENST00000645172.1:c.*1372A= ENSP00000495367.1:n.*1372A=
ENST00000646190.1:n.3001A=
ENST00000646208.1:c.1406A= ENSP00000493723.1:p.Lys469=
ENST00000646410.1:c.1541A= ENSP00000494205.1:p.Lys514=
ENST00000646562.1:c.*1504A= ENSP00000496087.1:n.*1504A=
ENST00000647468.2:c.1670A= MANE Select ENSP00000496731.1:p.Lys557=
ENST00000648111.1:c.*1358A= ENSP00000497275.1:n.*1358A=
ENST00000367101.5:c.*118A= ENSP00000356068.1:n.*118A=
ENST00000367104.7:c.1670A= ENSP00000356071.3:p.Lys557=
ENST00000435180.5:c.395A= ENSP00000391168.1:p.Lys132=
ENST00000606965.5:c.*231A= ENSP00000475808.1:n.*231A=
ENST00000607071.5:c.*1604A= ENSP00000475855.1:n.*1604A=
ENST00000607742.5:c.*2948A= ENSP00000475523.1:n.*2948A=
NM_032861.3:c.1670A= NP_116250.3:p.Lys557=
NR_073096.1:n.1603A=
XM_006715586.1:c.1460A= XP_006715649.1:p.Lys487=
XM_011536196.1:c.1649A= XP_011534498.1:p.Lys550=
XM_011536197.1:c.1556A= XP_011534499.1:p.Lys519=
XM_011536198.1:c.1460A= XP_011534500.1:p.Lys487=
XM_006715586.3:c.1460A= XP_006715649.1:p.Lys487=
XM_011536196.3:c.1649A= XP_011534498.1:p.Lys550=
XM_011536198.3:c.1460A= XP_011534500.1:p.Lys487=
XM_024446573.1:c.1670A= XP_024302341.1:p.Lys557=
XR_001743697.2:n.1701A=
XR_942606.2:n.1752A=
NM_032861.4:c.1670A= MANE Select NP_116250.3:p.Lys557=
NR_073096.2:n.1585A=