Canonical Allele Identifier: CA366250004
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158158353G>T , CM000668.2:g.158158353G>T GRCh38
NC_000006.11:g.158579385G>T , CM000668.1:g.158579385G>T GRCh37
NC_000006.10:g.158499373G>T NCBI36
NG_032889.1:g.14928C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.11C>A ENSP00000475855.1:p.Ala4Asp
ENST00000642244.1:c.11C>A ENSP00000493554.1:p.Ala4Asp
ENST00000642903.1:c.11C>A ENSP00000493559.1:p.Ala4Asp
ENST00000644972.1:c.11C>A ENSP00000496451.1:p.Ala4Asp
ENST00000645077.1:c.11C>A ENSP00000496113.1:p.Ala4Asp
ENST00000645172.1:c.11C>A ENSP00000495367.1:p.Ala4Asp
ENST00000646190.1:n.1279C>A
ENST00000646208.1:c.11C>A ENSP00000493723.1:p.Ala4Asp
ENST00000646410.1:c.11C>A ENSP00000494205.1:p.Ala4Asp
ENST00000646562.1:c.11C>A ENSP00000496087.1:p.Ala4Asp
ENST00000647468.2:c.11C>A MANE Select ENSP00000496731.1:p.Ala4Asp
ENST00000648111.1:c.11C>A ENSP00000497275.1:p.Ala4Asp
ENST00000367101.5:c.11C>A ENSP00000356068.1:p.Ala4Asp
ENST00000367104.7:c.11C>A ENSP00000356071.3:p.Ala4Asp
ENST00000606965.5:c.11C>A ENSP00000475808.1:p.Ala4Asp
ENST00000607000.1:c.11C>A ENSP00000475788.1:p.Ala4Asp
ENST00000607071.5:c.11C>A ENSP00000475855.1:p.Ala4Asp
ENST00000607742.5:c.11C>A ENSP00000475523.1:p.Ala4Asp
NM_032861.3:c.11C>A NP_116250.3:p.Ala4Asp
NR_073096.1:n.153C>A
XM_006715586.1:c.-163C>A XP_006715649.1:n.-163C>A
XM_011536196.1:c.27C>A XP_011534498.1:p.Gly9=
XM_011536197.1:c.11C>A XP_011534499.1:p.Ala4Asp
XR_942606.1:n.12C>A
XM_006715586.3:c.-163C>A XP_006715649.1:n.-163C>A
XM_011536196.3:c.27C>A XP_011534498.1:p.Gly9=
XM_024446573.1:c.11C>A XP_024302341.1:p.Ala4Asp
XR_001743697.2:n.129C>A
XR_942606.2:n.143C>A
NM_032861.4:c.11C>A MANE Select NP_116250.3:p.Ala4Asp
NR_073096.2:n.135C>A