Canonical Allele Identifier: CA366255119
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114899C>A , CM000668.2:g.158114899C>A GRCh38
NC_000006.11:g.158535931C>A , CM000668.1:g.158535931C>A GRCh37
NC_000006.10:g.158455919C>A NCBI36
NG_032889.1:g.58382G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.786G>T ENSP00000391168.2:n.786G>T
ENST00000607071.6:c.*1294G>T ENSP00000475855.1:n.*1294G>T
ENST00000642244.1:c.1484G>T ENSP00000493554.1:p.Arg495Ile
ENST00000642903.1:c.1574G>T ENSP00000493559.1:p.Arg525Ile
ENST00000644972.1:c.1574G>T ENSP00000496451.1:p.Arg525Ile
ENST00000645077.1:c.*1195G>T ENSP00000496113.1:n.*1195G>T
ENST00000645172.1:c.*1276G>T ENSP00000495367.1:n.*1276G>T
ENST00000646190.1:n.2905G>T
ENST00000646208.1:c.1310G>T ENSP00000493723.1:p.Arg437Ile
ENST00000646410.1:c.1445G>T ENSP00000494205.1:p.Arg482Ile
ENST00000646562.1:c.*1408G>T ENSP00000496087.1:n.*1408G>T
ENST00000647468.2:c.1574G>T MANE Select ENSP00000496731.1:p.Arg525Ile
ENST00000648111.1:c.*1262G>T ENSP00000497275.1:n.*1262G>T
ENST00000367101.5:c.*22G>T ENSP00000356068.1:n.*22G>T
ENST00000367104.7:c.1574G>T ENSP00000356071.3:p.Arg525Ile
ENST00000435180.5:c.299G>T ENSP00000391168.1:p.Arg100Ile
ENST00000606965.5:c.*135G>T ENSP00000475808.1:n.*135G>T
ENST00000607071.5:c.*1508G>T ENSP00000475855.1:n.*1508G>T
ENST00000607742.5:c.*2852G>T ENSP00000475523.1:n.*2852G>T
NM_032861.3:c.1574G>T NP_116250.3:p.Arg525Ile
NR_073096.1:n.1507G>T
XM_006715586.1:c.1364G>T XP_006715649.1:p.Arg455Ile
XM_011536196.1:c.1553G>T XP_011534498.1:p.Arg518Ile
XM_011536197.1:c.1460G>T XP_011534499.1:p.Arg487Ile
XM_011536198.1:c.1364G>T XP_011534500.1:p.Arg455Ile
XM_006715586.3:c.1364G>T XP_006715649.1:p.Arg455Ile
XM_011536196.3:c.1553G>T XP_011534498.1:p.Arg518Ile
XM_011536198.3:c.1364G>T XP_011534500.1:p.Arg455Ile
XM_024446573.1:c.1574G>T XP_024302341.1:p.Arg525Ile
XR_001743697.2:n.1605G>T
XR_942606.2:n.1656G>T
NM_032861.4:c.1574G>T MANE Select NP_116250.3:p.Arg525Ile
NR_073096.2:n.1489G>T