Canonical Allele Identifier: CA1675967743
Gene: SERAC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158158238T= , CM000668.2:g.158158238T= GRCh38
NC_000006.11:g.158579270T= , CM000668.1:g.158579270T= GRCh37
NC_000006.10:g.158499258T= NCBI36
NG_032889.1:g.15043A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.91+35A= ENSP00000475855.1:n.91+35A=
ENST00000642244.1:c.91+35A= ENSP00000493554.1:n.91+35A=
ENST00000642903.1:c.91+35A= ENSP00000493559.1:n.91+35A=
ENST00000644972.1:c.91+35A= ENSP00000496451.1:n.91+35A=
ENST00000645077.1:c.91+35A= ENSP00000496113.1:n.91+35A=
ENST00000645172.1:c.91+35A= ENSP00000495367.1:n.91+35A=
ENST00000646190.1:n.1359+35A=
ENST00000646208.1:c.91+35A= ENSP00000493723.1:n.91+35A=
ENST00000646410.1:c.91+35A= ENSP00000494205.1:n.91+35A=
ENST00000646562.1:c.91+35A= ENSP00000496087.1:n.91+35A=
ENST00000647468.2:c.91+35A= MANE Select ENSP00000496731.1:n.91+35A=
ENST00000648111.1:c.91+35A= ENSP00000497275.1:n.91+35A=
ENST00000367101.5:c.91+35A= ENSP00000356068.1:n.91+35A=
ENST00000367104.7:c.91+35A= ENSP00000356071.3:n.91+35A=
ENST00000606965.5:c.91+35A= ENSP00000475808.1:n.91+35A=
ENST00000607000.1:c.91+35A= ENSP00000475788.1:n.91+35A=
ENST00000607071.5:c.91+35A= ENSP00000475855.1:n.91+35A=
ENST00000607742.5:c.91+35A= ENSP00000475523.1:n.91+35A=
NM_032861.3:c.91+35A= NP_116250.3:n.91+35A=
NR_073096.1:n.233+35A=
XM_006715586.1:c.-83+35A= XP_006715649.1:n.-83+35A=
XM_011536196.1:c.107+35A= XP_011534498.1:n.107+35A=
XM_011536197.1:c.91+35A= XP_011534499.1:n.91+35A=
XR_942606.1:n.92+35A=
XM_006715586.3:c.-83+35A= XP_006715649.1:n.-83+35A=
XM_011536196.3:c.107+35A= XP_011534498.1:n.107+35A=
XM_024446573.1:c.91+35A= XP_024302341.1:n.91+35A=
XR_001743697.2:n.209+35A=
XR_942606.2:n.223+35A=
NM_032861.4:c.91+35A= MANE Select NP_116250.3:n.91+35A=
NR_073096.2:n.215+35A=