Canonical Allele Identifier: CA366254598
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114713G>C , CM000668.2:g.158114713G>C GRCh38
NC_000006.11:g.158535745G>C , CM000668.1:g.158535745G>C GRCh37
NC_000006.10:g.158455733G>C NCBI36
NG_032889.1:g.58568C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+76C>G ENSP00000475855.1:n.*1404+76C>G
ENST00000642244.1:c.1594+76C>G ENSP00000493554.1:n.1594+76C>G
ENST00000642903.1:c.1760C>G ENSP00000493559.1:p.Pro587Arg
ENST00000644972.1:c.1684+76C>G ENSP00000496451.1:n.1684+76C>G
ENST00000645077.1:c.*1305+76C>G ENSP00000496113.1:n.*1305+76C>G
ENST00000645172.1:c.*1386+76C>G ENSP00000495367.1:n.*1386+76C>G
ENST00000646190.1:n.3015+76C>G
ENST00000646208.1:c.1420+76C>G ENSP00000493723.1:n.1420+76C>G
ENST00000646410.1:c.1555+76C>G ENSP00000494205.1:n.1555+76C>G
ENST00000646562.1:c.*1594C>G ENSP00000496087.1:n.*1594C>G
ENST00000647468.2:c.1684+76C>G MANE Select ENSP00000496731.1:n.1684+76C>G
ENST00000648111.1:c.*1372+76C>G ENSP00000497275.1:n.*1372+76C>G
ENST00000367104.7:c.1684+76C>G ENSP00000356071.3:n.1684+76C>G
ENST00000435180.5:c.485C>G ENSP00000391168.1:p.Pro162Arg
ENST00000606965.5:c.*321C>G ENSP00000475808.1:n.*321C>G
ENST00000607071.5:c.*1618+76C>G ENSP00000475855.1:n.*1618+76C>G
ENST00000607742.5:c.*2962+76C>G ENSP00000475523.1:n.*2962+76C>G
NM_032861.3:c.1684+76C>G NP_116250.3:n.1684+76C>G
NR_073096.1:n.1693C>G
XM_006715586.1:c.1474+76C>G XP_006715649.1:n.1474+76C>G
XM_011536196.1:c.1663+76C>G XP_011534498.1:n.1663+76C>G
XM_011536197.1:c.1570+76C>G XP_011534499.1:n.1570+76C>G
XM_011536198.1:c.1474+76C>G XP_011534500.1:n.1474+76C>G
XM_006715586.3:c.1474+76C>G XP_006715649.1:n.1474+76C>G
XM_011536196.3:c.1663+76C>G XP_011534498.1:n.1663+76C>G
XM_011536198.3:c.1474+76C>G XP_011534500.1:n.1474+76C>G
XM_024446573.1:c.1684+76C>G XP_024302341.1:n.1684+76C>G
XR_001743697.2:n.1715+76C>G
XR_942606.2:n.1766+76C>G
NM_032861.4:c.1684+76C>G MANE Select NP_116250.3:n.1684+76C>G
NR_073096.2:n.1675C>G