Canonical Allele Identifier: CA1675959267

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784238066

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114755_158114756del , CM000668.2:g.158114755_158114756del	GRCh38
NC_000006.11:g.158535787_158535788del , CM000668.1:g.158535787_158535788del	GRCh37
NC_000006.10:g.158455775_158455776del	NCBI36
NG_032889.1:g.58528_58529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+36_*1404+37del	ENSP00000475855.1:n.*1404+36_*1404+37del
ENST00000642244.1:c.1594+36_1594+37del	ENSP00000493554.1:n.1594+36_1594+37del
ENST00000642903.1:c.1720_1721del	ENSP00000493559.1:p.Ile574Ter
ENST00000644972.1:c.1684+36_1684+37del	ENSP00000496451.1:n.1684+36_1684+37del
ENST00000645077.1:c.*1305+36_*1305+37del	ENSP00000496113.1:n.*1305+36_*1305+37del
ENST00000645172.1:c.*1386+36_*1386+37del	ENSP00000495367.1:n.*1386+36_*1386+37del
ENST00000646190.1:n.3015+36_3015+37del
ENST00000646208.1:c.1420+36_1420+37del	ENSP00000493723.1:n.1420+36_1420+37del
ENST00000646410.1:c.1555+36_1555+37del	ENSP00000494205.1:n.1555+36_1555+37del
ENST00000646562.1:c.*1554_*1555del	ENSP00000496087.1:n.*1554_*1555del
ENST00000647468.2:c.1684+36_1684+37del MANE Select	ENSP00000496731.1:n.1684+36_1684+37del
ENST00000648111.1:c.*1372+36_*1372+37del	ENSP00000497275.1:n.*1372+36_*1372+37del
ENST00000367101.5:c.*168_*169del	ENSP00000356068.1:n.*168_*169del
ENST00000367104.7:c.1684+36_1684+37del	ENSP00000356071.3:n.1684+36_1684+37del
ENST00000435180.5:c.445_446del	ENSP00000391168.1:p.Ile149Ter
ENST00000606965.5:c.*281_*282del	ENSP00000475808.1:n.*281_*282del
ENST00000607071.5:c.*1618+36_*1618+37del	ENSP00000475855.1:n.*1618+36_*1618+37del
ENST00000607742.5:c.*2962+36_*2962+37del	ENSP00000475523.1:n.*2962+36_*2962+37del
NM_032861.3:c.1684+36_1684+37del	NP_116250.3:n.1684+36_1684+37del
NR_073096.1:n.1653_1654del
XM_006715586.1:c.1474+36_1474+37del	XP_006715649.1:n.1474+36_1474+37del
XM_011536196.1:c.1663+36_1663+37del	XP_011534498.1:n.1663+36_1663+37del
XM_011536197.1:c.1570+36_1570+37del	XP_011534499.1:n.1570+36_1570+37del
XM_011536198.1:c.1474+36_1474+37del	XP_011534500.1:n.1474+36_1474+37del
XM_006715586.3:c.1474+36_1474+37del	XP_006715649.1:n.1474+36_1474+37del
XM_011536196.3:c.1663+36_1663+37del	XP_011534498.1:n.1663+36_1663+37del
XM_011536198.3:c.1474+36_1474+37del	XP_011534500.1:n.1474+36_1474+37del
XM_024446573.1:c.1684+36_1684+37del	XP_024302341.1:n.1684+36_1684+37del
XR_001743697.2:n.1715+36_1715+37del
XR_942606.2:n.1766+36_1766+37del
NM_032861.4:c.1684+36_1684+37del MANE Select	NP_116250.3:n.1684+36_1684+37del
NR_073096.2:n.1635_1636del