Canonical Allele Identifier: CA452820155
Gene: SERAC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.158535915A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114883A>G , CM000668.2:g.158114883A>G GRCh38
NC_000006.11:g.158535915A>G , CM000668.1:g.158535915A>G GRCh37
NC_000006.10:g.158455903A>G NCBI36
NG_032889.1:g.58398T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435180.6:c.802T>C ENSP00000391168.2:n.802T>C
ENST00000607071.6:c.*1310T>C ENSP00000475855.1:n.*1310T>C
ENST00000642244.1:c.1500T>C ENSP00000493554.1:p.Tyr500=
ENST00000642903.1:c.1590T>C ENSP00000493559.1:p.Tyr530=
ENST00000644972.1:c.1590T>C ENSP00000496451.1:p.Tyr530=
ENST00000645077.1:c.*1211T>C ENSP00000496113.1:n.*1211T>C
ENST00000645172.1:c.*1292T>C ENSP00000495367.1:n.*1292T>C
ENST00000646190.1:n.2921T>C
ENST00000646208.1:c.1326T>C ENSP00000493723.1:p.Tyr442=
ENST00000646410.1:c.1461T>C ENSP00000494205.1:p.Tyr487=
ENST00000646562.1:c.*1424T>C ENSP00000496087.1:n.*1424T>C
ENST00000647468.2:c.1590T>C MANE Select ENSP00000496731.1:p.Tyr530=
ENST00000648111.1:c.*1278T>C ENSP00000497275.1:n.*1278T>C
ENST00000367101.5:c.*38T>C ENSP00000356068.1:n.*38T>C
ENST00000367104.7:c.1590T>C ENSP00000356071.3:p.Tyr530=
ENST00000435180.5:c.315T>C ENSP00000391168.1:p.Tyr105=
ENST00000606965.5:c.*151T>C ENSP00000475808.1:n.*151T>C
ENST00000607071.5:c.*1524T>C ENSP00000475855.1:n.*1524T>C
ENST00000607742.5:c.*2868T>C ENSP00000475523.1:n.*2868T>C
NM_032861.3:c.1590T>C NP_116250.3:p.Tyr530=
NR_073096.1:n.1523T>C
XM_006715586.1:c.1380T>C XP_006715649.1:p.Tyr460=
XM_011536196.1:c.1569T>C XP_011534498.1:p.Tyr523=
XM_011536197.1:c.1476T>C XP_011534499.1:p.Tyr492=
XM_011536198.1:c.1380T>C XP_011534500.1:p.Tyr460=
XM_006715586.3:c.1380T>C XP_006715649.1:p.Tyr460=
XM_011536196.3:c.1569T>C XP_011534498.1:p.Tyr523=
XM_011536198.3:c.1380T>C XP_011534500.1:p.Tyr460=
XM_024446573.1:c.1590T>C XP_024302341.1:p.Tyr530=
XR_001743697.2:n.1621T>C
XR_942606.2:n.1672T>C
NM_032861.4:c.1590T>C MANE Select NP_116250.3:p.Tyr530=
NR_073096.2:n.1505T>C