Canonical Allele Identifier: CA366254956
Gene: SERAC1 HGNC NCBI

Linked Data

dbSNP Id: rs1297861569

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114824A>T , CM000668.2:g.158114824A>T GRCh38
NC_000006.11:g.158535856A>T , CM000668.1:g.158535856A>T GRCh37
NC_000006.10:g.158455844A>T NCBI36
NG_032889.1:g.58457T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1369T>A ENSP00000475855.1:n.*1369T>A
ENST00000642244.1:c.1559T>A ENSP00000493554.1:p.Leu520His
ENST00000642903.1:c.1649T>A ENSP00000493559.1:p.Leu550His
ENST00000644972.1:c.1649T>A ENSP00000496451.1:p.Leu550His
ENST00000645077.1:c.*1270T>A ENSP00000496113.1:n.*1270T>A
ENST00000645172.1:c.*1351T>A ENSP00000495367.1:n.*1351T>A
ENST00000646190.1:n.2980T>A
ENST00000646208.1:c.1385T>A ENSP00000493723.1:p.Leu462His
ENST00000646410.1:c.1520T>A ENSP00000494205.1:p.Leu507His
ENST00000646562.1:c.*1483T>A ENSP00000496087.1:n.*1483T>A
ENST00000647468.2:c.1649T>A MANE Select ENSP00000496731.1:p.Leu550His
ENST00000648111.1:c.*1337T>A ENSP00000497275.1:n.*1337T>A
ENST00000367101.5:c.*97T>A ENSP00000356068.1:n.*97T>A
ENST00000367104.7:c.1649T>A ENSP00000356071.3:p.Leu550His
ENST00000435180.5:c.374T>A ENSP00000391168.1:p.Leu125His
ENST00000606965.5:c.*210T>A ENSP00000475808.1:n.*210T>A
ENST00000607071.5:c.*1583T>A ENSP00000475855.1:n.*1583T>A
ENST00000607742.5:c.*2927T>A ENSP00000475523.1:n.*2927T>A
NM_032861.3:c.1649T>A NP_116250.3:p.Leu550His
NR_073096.1:n.1582T>A
XM_006715586.1:c.1439T>A XP_006715649.1:p.Leu480His
XM_011536196.1:c.1628T>A XP_011534498.1:p.Leu543His
XM_011536197.1:c.1535T>A XP_011534499.1:p.Leu512His
XM_011536198.1:c.1439T>A XP_011534500.1:p.Leu480His
XM_006715586.3:c.1439T>A XP_006715649.1:p.Leu480His
XM_011536196.3:c.1628T>A XP_011534498.1:p.Leu543His
XM_011536198.3:c.1439T>A XP_011534500.1:p.Leu480His
XM_024446573.1:c.1649T>A XP_024302341.1:p.Leu550His
XR_001743697.2:n.1680T>A
XR_942606.2:n.1731T>A
NM_032861.4:c.1649T>A MANE Select NP_116250.3:p.Leu550His
NR_073096.2:n.1564T>A