Canonical Allele Identifier: CA150914421
Gene: SERAC1 HGNC NCBI

Linked Data

dbSNP Id: rs201763787

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114688T>A , CM000668.2:g.158114688T>A GRCh38
NC_000006.11:g.158535720T>A , CM000668.1:g.158535720T>A GRCh37
NC_000006.10:g.158455708T>A NCBI36
NG_032889.1:g.58593A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+101A>T ENSP00000475855.1:n.*1404+101A>T
ENST00000642244.1:c.1594+101A>T ENSP00000493554.1:n.1594+101A>T
ENST00000642903.1:c.*21A>T ENSP00000493559.1:n.*21A>T
ENST00000644972.1:c.1684+101A>T ENSP00000496451.1:n.1684+101A>T
ENST00000645077.1:c.*1305+101A>T ENSP00000496113.1:n.*1305+101A>T
ENST00000645172.1:c.*1386+101A>T ENSP00000495367.1:n.*1386+101A>T
ENST00000646190.1:n.3015+101A>T
ENST00000646208.1:c.1420+101A>T ENSP00000493723.1:n.1420+101A>T
ENST00000646410.1:c.1555+101A>T ENSP00000494205.1:n.1555+101A>T
ENST00000646562.1:c.*1619A>T ENSP00000496087.1:n.*1619A>T
ENST00000647468.2:c.1684+101A>T MANE Select ENSP00000496731.1:n.1684+101A>T
ENST00000648111.1:c.*1372+101A>T ENSP00000497275.1:n.*1372+101A>T
ENST00000367104.7:c.1684+101A>T ENSP00000356071.3:n.1684+101A>T
ENST00000606965.5:c.*346A>T ENSP00000475808.1:n.*346A>T
ENST00000607071.5:c.*1618+101A>T ENSP00000475855.1:n.*1618+101A>T
ENST00000607742.5:c.*2962+101A>T ENSP00000475523.1:n.*2962+101A>T
NM_032861.3:c.1684+101A>T NP_116250.3:n.1684+101A>T
NR_073096.1:n.1718A>T
XM_006715586.1:c.1474+101A>T XP_006715649.1:n.1474+101A>T
XM_011536196.1:c.1663+101A>T XP_011534498.1:n.1663+101A>T
XM_011536197.1:c.1570+101A>T XP_011534499.1:n.1570+101A>T
XM_011536198.1:c.1474+101A>T XP_011534500.1:n.1474+101A>T
XM_006715586.3:c.1474+101A>T XP_006715649.1:n.1474+101A>T
XM_011536196.3:c.1663+101A>T XP_011534498.1:n.1663+101A>T
XM_011536198.3:c.1474+101A>T XP_011534500.1:n.1474+101A>T
XM_024446573.1:c.1684+101A>T XP_024302341.1:n.1684+101A>T
XR_001743697.2:n.1715+101A>T
XR_942606.2:n.1766+101A>T
NM_032861.4:c.1684+101A>T MANE Select NP_116250.3:n.1684+101A>T
NR_073096.2:n.1700A>T