Canonical Allele Identifier: CA366255018
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114854G>A , CM000668.2:g.158114854G>A GRCh38
NC_000006.11:g.158535886G>A , CM000668.1:g.158535886G>A GRCh37
NC_000006.10:g.158455874G>A NCBI36
NG_032889.1:g.58427C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435180.6:c.831C>T ENSP00000391168.2:n.831C>T
ENST00000607071.6:c.*1339C>T ENSP00000475855.1:n.*1339C>T
ENST00000642244.1:c.1529C>T ENSP00000493554.1:p.Ala510Val
ENST00000642903.1:c.1619C>T ENSP00000493559.1:p.Ala540Val
ENST00000644972.1:c.1619C>T ENSP00000496451.1:p.Ala540Val
ENST00000645077.1:c.*1240C>T ENSP00000496113.1:n.*1240C>T
ENST00000645172.1:c.*1321C>T ENSP00000495367.1:n.*1321C>T
ENST00000646190.1:n.2950C>T
ENST00000646208.1:c.1355C>T ENSP00000493723.1:p.Ala452Val
ENST00000646410.1:c.1490C>T ENSP00000494205.1:p.Ala497Val
ENST00000646562.1:c.*1453C>T ENSP00000496087.1:n.*1453C>T
ENST00000647468.2:c.1619C>T MANE Select ENSP00000496731.1:p.Ala540Val
ENST00000648111.1:c.*1307C>T ENSP00000497275.1:n.*1307C>T
ENST00000367101.5:c.*67C>T ENSP00000356068.1:n.*67C>T
ENST00000367104.7:c.1619C>T ENSP00000356071.3:p.Ala540Val
ENST00000435180.5:c.344C>T ENSP00000391168.1:p.Ala115Val
ENST00000606965.5:c.*180C>T ENSP00000475808.1:n.*180C>T
ENST00000607071.5:c.*1553C>T ENSP00000475855.1:n.*1553C>T
ENST00000607742.5:c.*2897C>T ENSP00000475523.1:n.*2897C>T
NM_032861.3:c.1619C>T NP_116250.3:p.Ala540Val
NR_073096.1:n.1552C>T
XM_006715586.1:c.1409C>T XP_006715649.1:p.Ala470Val
XM_011536196.1:c.1598C>T XP_011534498.1:p.Ala533Val
XM_011536197.1:c.1505C>T XP_011534499.1:p.Ala502Val
XM_011536198.1:c.1409C>T XP_011534500.1:p.Ala470Val
XM_006715586.3:c.1409C>T XP_006715649.1:p.Ala470Val
XM_011536196.3:c.1598C>T XP_011534498.1:p.Ala533Val
XM_011536198.3:c.1409C>T XP_011534500.1:p.Ala470Val
XM_024446573.1:c.1619C>T XP_024302341.1:p.Ala540Val
XR_001743697.2:n.1650C>T
XR_942606.2:n.1701C>T
NM_032861.4:c.1619C>T MANE Select NP_116250.3:p.Ala540Val
NR_073096.2:n.1534C>T