Canonical Allele Identifier: CA366255004
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114848T>A , CM000668.2:g.158114848T>A GRCh38
NC_000006.11:g.158535880T>A , CM000668.1:g.158535880T>A GRCh37
NC_000006.10:g.158455868T>A NCBI36
NG_032889.1:g.58433A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.837A>T ENSP00000391168.2:n.837A>T
ENST00000607071.6:c.*1345A>T ENSP00000475855.1:n.*1345A>T
ENST00000642244.1:c.1535A>T ENSP00000493554.1:p.Tyr512Phe
ENST00000642903.1:c.1625A>T ENSP00000493559.1:p.Tyr542Phe
ENST00000644972.1:c.1625A>T ENSP00000496451.1:p.Tyr542Phe
ENST00000645077.1:c.*1246A>T ENSP00000496113.1:n.*1246A>T
ENST00000645172.1:c.*1327A>T ENSP00000495367.1:n.*1327A>T
ENST00000646190.1:n.2956A>T
ENST00000646208.1:c.1361A>T ENSP00000493723.1:p.Tyr454Phe
ENST00000646410.1:c.1496A>T ENSP00000494205.1:p.Tyr499Phe
ENST00000646562.1:c.*1459A>T ENSP00000496087.1:n.*1459A>T
ENST00000647468.2:c.1625A>T MANE Select ENSP00000496731.1:p.Tyr542Phe
ENST00000648111.1:c.*1313A>T ENSP00000497275.1:n.*1313A>T
ENST00000367101.5:c.*73A>T ENSP00000356068.1:n.*73A>T
ENST00000367104.7:c.1625A>T ENSP00000356071.3:p.Tyr542Phe
ENST00000435180.5:c.350A>T ENSP00000391168.1:p.Tyr117Phe
ENST00000606965.5:c.*186A>T ENSP00000475808.1:n.*186A>T
ENST00000607071.5:c.*1559A>T ENSP00000475855.1:n.*1559A>T
ENST00000607742.5:c.*2903A>T ENSP00000475523.1:n.*2903A>T
NM_032861.3:c.1625A>T NP_116250.3:p.Tyr542Phe
NR_073096.1:n.1558A>T
XM_006715586.1:c.1415A>T XP_006715649.1:p.Tyr472Phe
XM_011536196.1:c.1604A>T XP_011534498.1:p.Tyr535Phe
XM_011536197.1:c.1511A>T XP_011534499.1:p.Tyr504Phe
XM_011536198.1:c.1415A>T XP_011534500.1:p.Tyr472Phe
XM_006715586.3:c.1415A>T XP_006715649.1:p.Tyr472Phe
XM_011536196.3:c.1604A>T XP_011534498.1:p.Tyr535Phe
XM_011536198.3:c.1415A>T XP_011534500.1:p.Tyr472Phe
XM_024446573.1:c.1625A>T XP_024302341.1:p.Tyr542Phe
XR_001743697.2:n.1656A>T
XR_942606.2:n.1707A>T
NM_032861.4:c.1625A>T MANE Select NP_116250.3:p.Tyr542Phe
NR_073096.2:n.1540A>T