Canonical Allele Identifier: CA1675959050

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114593_158114596delinsAAAT , CM000668.2:g.158114593_158114596delinsAAAT	GRCh38
NC_000006.11:g.158535625_158535628delinsAAAT , CM000668.1:g.158535625_158535628delinsAAAT	GRCh37
NC_000006.10:g.158455613_158455616delinsAAAT	NCBI36
NG_032889.1:g.58685_58688delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+193_*1404+196delinsATTT	ENSP00000475855.1:n.*1404+193_*1404+196delinsATTT
ENST00000642244.1:c.1594+193_1594+196delinsATTT	ENSP00000493554.1:n.1594+193_1594+196delinsATTT
ENST00000642903.1:c.*113_*116delinsATTT	ENSP00000493559.1:n.*113_*116delinsATTT
ENST00000644972.1:c.1684+193_1684+196delinsATTT	ENSP00000496451.1:n.1684+193_1684+196delinsATTT
ENST00000645077.1:c.*1305+193_*1305+196delinsATTT	ENSP00000496113.1:n.*1305+193_*1305+196delinsATTT
ENST00000645172.1:c.*1386+193_*1386+196delinsATTT	ENSP00000495367.1:n.*1386+193_*1386+196delinsATTT
ENST00000646190.1:n.3015+193_3015+196delinsATTT
ENST00000646208.1:c.1420+193_1420+196delinsATTT	ENSP00000493723.1:n.1420+193_1420+196delinsATTT
ENST00000646410.1:c.1555+193_1555+196delinsATTT	ENSP00000494205.1:n.1555+193_1555+196delinsATTT
ENST00000646562.1:c.*1711_*1714delinsATTT	ENSP00000496087.1:n.*1711_*1714delinsATTT
ENST00000647468.2:c.1684+193_1684+196delinsATTT MANE Select	ENSP00000496731.1:n.1684+193_1684+196delinsATTT
ENST00000648111.1:c.*1372+193_*1372+196delinsATTT	ENSP00000497275.1:n.*1372+193_*1372+196delinsATTT
ENST00000367104.7:c.1684+193_1684+196delinsATTT	ENSP00000356071.3:n.1684+193_1684+196delinsATTT
ENST00000606965.5:c.*438_*441delinsATTT	ENSP00000475808.1:n.*438_*441delinsATTT
ENST00000607071.5:c.*1618+193_*1618+196delinsATTT	ENSP00000475855.1:n.*1618+193_*1618+196delinsATTT
ENST00000607742.5:c.*2962+193_*2962+196delinsATTT	ENSP00000475523.1:n.*2962+193_*2962+196delinsATTT
NM_032861.3:c.1684+193_1684+196delinsATTT	NP_116250.3:n.1684+193_1684+196delinsATTT
NR_073096.1:n.1810_1813delinsATTT
XM_006715586.1:c.1474+193_1474+196delinsATTT	XP_006715649.1:n.1474+193_1474+196delinsATTT
XM_011536196.1:c.1663+193_1663+196delinsATTT	XP_011534498.1:n.1663+193_1663+196delinsATTT
XM_011536197.1:c.1570+193_1570+196delinsATTT	XP_011534499.1:n.1570+193_1570+196delinsATTT
XM_011536198.1:c.1474+193_1474+196delinsATTT	XP_011534500.1:n.1474+193_1474+196delinsATTT
XM_006715586.3:c.1474+193_1474+196delinsATTT	XP_006715649.1:n.1474+193_1474+196delinsATTT
XM_011536196.3:c.1663+193_1663+196delinsATTT	XP_011534498.1:n.1663+193_1663+196delinsATTT
XM_011536198.3:c.1474+193_1474+196delinsATTT	XP_011534500.1:n.1474+193_1474+196delinsATTT
XM_024446573.1:c.1684+193_1684+196delinsATTT	XP_024302341.1:n.1684+193_1684+196delinsATTT
XR_001743697.2:n.1715+193_1715+196delinsATTT
XR_942606.2:n.1766+193_1766+196delinsATTT
NM_032861.4:c.1684+193_1684+196delinsATTT MANE Select	NP_116250.3:n.1684+193_1684+196delinsATTT
NR_073096.2:n.1792_1795delinsATTT