Canonical Allele Identifier: CA1675959263

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114751_158114753delinsAAT , CM000668.2:g.158114751_158114753delinsAAT	GRCh38
NC_000006.11:g.158535783_158535785delinsAAT , CM000668.1:g.158535783_158535785delinsAAT	GRCh37
NC_000006.10:g.158455771_158455773delinsAAT	NCBI36
NG_032889.1:g.58528_58530delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+36_*1404+38delinsATT	ENSP00000475855.1:n.*1404+36_*1404+38delinsATT
ENST00000642244.1:c.1594+36_1594+38delinsATT	ENSP00000493554.1:n.1594+36_1594+38delinsATT
ENST00000642903.1:c.1720_1722delinsATT	ENSP00000493559.1:p.Ile574=
ENST00000644972.1:c.1684+36_1684+38delinsATT	ENSP00000496451.1:n.1684+36_1684+38delinsATT
ENST00000645077.1:c.*1305+36_*1305+38delinsATT	ENSP00000496113.1:n.*1305+36_*1305+38delinsATT
ENST00000645172.1:c.*1386+36_*1386+38delinsATT	ENSP00000495367.1:n.*1386+36_*1386+38delinsATT
ENST00000646190.1:n.3015+36_3015+38delinsATT
ENST00000646208.1:c.1420+36_1420+38delinsATT	ENSP00000493723.1:n.1420+36_1420+38delinsATT
ENST00000646410.1:c.1555+36_1555+38delinsATT	ENSP00000494205.1:n.1555+36_1555+38delinsATT
ENST00000646562.1:c.*1554_*1556delinsATT	ENSP00000496087.1:n.*1554_*1556delinsATT
ENST00000647468.2:c.1684+36_1684+38delinsATT MANE Select	ENSP00000496731.1:n.1684+36_1684+38delinsATT
ENST00000648111.1:c.*1372+36_*1372+38delinsATT	ENSP00000497275.1:n.*1372+36_*1372+38delinsATT
ENST00000367101.5:c.*168_*170delinsATT	ENSP00000356068.1:n.*168_*170delinsATT
ENST00000367104.7:c.1684+36_1684+38delinsATT	ENSP00000356071.3:n.1684+36_1684+38delinsATT
ENST00000435180.5:c.445_447delinsATT	ENSP00000391168.1:p.Ile149=
ENST00000606965.5:c.*281_*283delinsATT	ENSP00000475808.1:n.*281_*283delinsATT
ENST00000607071.5:c.*1618+36_*1618+38delinsATT	ENSP00000475855.1:n.*1618+36_*1618+38delinsATT
ENST00000607742.5:c.*2962+36_*2962+38delinsATT	ENSP00000475523.1:n.*2962+36_*2962+38delinsATT
NM_032861.3:c.1684+36_1684+38delinsATT	NP_116250.3:n.1684+36_1684+38delinsATT
NR_073096.1:n.1653_1655delinsATT
XM_006715586.1:c.1474+36_1474+38delinsATT	XP_006715649.1:n.1474+36_1474+38delinsATT
XM_011536196.1:c.1663+36_1663+38delinsATT	XP_011534498.1:n.1663+36_1663+38delinsATT
XM_011536197.1:c.1570+36_1570+38delinsATT	XP_011534499.1:n.1570+36_1570+38delinsATT
XM_011536198.1:c.1474+36_1474+38delinsATT	XP_011534500.1:n.1474+36_1474+38delinsATT
XM_006715586.3:c.1474+36_1474+38delinsATT	XP_006715649.1:n.1474+36_1474+38delinsATT
XM_011536196.3:c.1663+36_1663+38delinsATT	XP_011534498.1:n.1663+36_1663+38delinsATT
XM_011536198.3:c.1474+36_1474+38delinsATT	XP_011534500.1:n.1474+36_1474+38delinsATT
XM_024446573.1:c.1684+36_1684+38delinsATT	XP_024302341.1:n.1684+36_1684+38delinsATT
XR_001743697.2:n.1715+36_1715+38delinsATT
XR_942606.2:n.1766+36_1766+38delinsATT
NM_032861.4:c.1684+36_1684+38delinsATT MANE Select	NP_116250.3:n.1684+36_1684+38delinsATT
NR_073096.2:n.1635_1637delinsATT