Canonical Allele Identifier: CA1675959105

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114660_158114661delinsGA , CM000668.2:g.158114660_158114661delinsGA	GRCh38
NC_000006.11:g.158535692_158535693delinsGA , CM000668.1:g.158535692_158535693delinsGA	GRCh37
NC_000006.10:g.158455680_158455681delinsGA	NCBI36
NG_032889.1:g.58620_58621delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+128_*1404+129delinsTC	ENSP00000475855.1:n.*1404+128_*1404+129delinsTC
ENST00000642244.1:c.1594+128_1594+129delinsTC	ENSP00000493554.1:n.1594+128_1594+129delinsTC
ENST00000642903.1:c.*48_*49delinsTC	ENSP00000493559.1:n.*48_*49delinsTC
ENST00000644972.1:c.1684+128_1684+129delinsTC	ENSP00000496451.1:n.1684+128_1684+129delinsTC
ENST00000645077.1:c.*1305+128_*1305+129delinsTC	ENSP00000496113.1:n.*1305+128_*1305+129delinsTC
ENST00000645172.1:c.*1386+128_*1386+129delinsTC	ENSP00000495367.1:n.*1386+128_*1386+129delinsTC
ENST00000646190.1:n.3015+128_3015+129delinsTC
ENST00000646208.1:c.1420+128_1420+129delinsTC	ENSP00000493723.1:n.1420+128_1420+129delinsTC
ENST00000646410.1:c.1555+128_1555+129delinsTC	ENSP00000494205.1:n.1555+128_1555+129delinsTC
ENST00000646562.1:c.*1646_*1647delinsTC	ENSP00000496087.1:n.*1646_*1647delinsTC
ENST00000647468.2:c.1684+128_1684+129delinsTC MANE Select	ENSP00000496731.1:n.1684+128_1684+129delinsTC
ENST00000648111.1:c.*1372+128_*1372+129delinsTC	ENSP00000497275.1:n.*1372+128_*1372+129delinsTC
ENST00000367104.7:c.1684+128_1684+129delinsTC	ENSP00000356071.3:n.1684+128_1684+129delinsTC
ENST00000606965.5:c.*373_*374delinsTC	ENSP00000475808.1:n.*373_*374delinsTC
ENST00000607071.5:c.*1618+128_*1618+129delinsTC	ENSP00000475855.1:n.*1618+128_*1618+129delinsTC
ENST00000607742.5:c.*2962+128_*2962+129delinsTC	ENSP00000475523.1:n.*2962+128_*2962+129delinsTC
NM_032861.3:c.1684+128_1684+129delinsTC	NP_116250.3:n.1684+128_1684+129delinsTC
NR_073096.1:n.1745_1746delinsTC
XM_006715586.1:c.1474+128_1474+129delinsTC	XP_006715649.1:n.1474+128_1474+129delinsTC
XM_011536196.1:c.1663+128_1663+129delinsTC	XP_011534498.1:n.1663+128_1663+129delinsTC
XM_011536197.1:c.1570+128_1570+129delinsTC	XP_011534499.1:n.1570+128_1570+129delinsTC
XM_011536198.1:c.1474+128_1474+129delinsTC	XP_011534500.1:n.1474+128_1474+129delinsTC
XM_006715586.3:c.1474+128_1474+129delinsTC	XP_006715649.1:n.1474+128_1474+129delinsTC
XM_011536196.3:c.1663+128_1663+129delinsTC	XP_011534498.1:n.1663+128_1663+129delinsTC
XM_011536198.3:c.1474+128_1474+129delinsTC	XP_011534500.1:n.1474+128_1474+129delinsTC
XM_024446573.1:c.1684+128_1684+129delinsTC	XP_024302341.1:n.1684+128_1684+129delinsTC
XR_001743697.2:n.1715+128_1715+129delinsTC
XR_942606.2:n.1766+128_1766+129delinsTC
NM_032861.4:c.1684+128_1684+129delinsTC MANE Select	NP_116250.3:n.1684+128_1684+129delinsTC
NR_073096.2:n.1727_1728delinsTC