Canonical Allele Identifier: CA1675959056

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784231468
• gnomAD v4: 6-158114598-ATGGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114600_158114604del , CM000668.2:g.158114600_158114604del	GRCh38
NC_000006.11:g.158535632_158535636del , CM000668.1:g.158535632_158535636del	GRCh37
NC_000006.10:g.158455620_158455624del	NCBI36
NG_032889.1:g.58678_58682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+186_*1404+190del	ENSP00000475855.1:n.*1404+186_*1404+190del
ENST00000642244.1:c.1594+186_1594+190del	ENSP00000493554.1:n.1594+186_1594+190del
ENST00000642903.1:c.*106_*110del	ENSP00000493559.1:n.*106_*110del
ENST00000644972.1:c.1684+186_1684+190del	ENSP00000496451.1:n.1684+186_1684+190del
ENST00000645077.1:c.*1305+186_*1305+190del	ENSP00000496113.1:n.*1305+186_*1305+190del
ENST00000645172.1:c.*1386+186_*1386+190del	ENSP00000495367.1:n.*1386+186_*1386+190del
ENST00000646190.1:n.3015+186_3015+190del
ENST00000646208.1:c.1420+186_1420+190del	ENSP00000493723.1:n.1420+186_1420+190del
ENST00000646410.1:c.1555+186_1555+190del	ENSP00000494205.1:n.1555+186_1555+190del
ENST00000646562.1:c.*1704_*1708del	ENSP00000496087.1:n.*1704_*1708del
ENST00000647468.2:c.1684+186_1684+190del MANE Select	ENSP00000496731.1:n.1684+186_1684+190del
ENST00000648111.1:c.*1372+186_*1372+190del	ENSP00000497275.1:n.*1372+186_*1372+190del
ENST00000367104.7:c.1684+186_1684+190del	ENSP00000356071.3:n.1684+186_1684+190del
ENST00000606965.5:c.*431_*435del	ENSP00000475808.1:n.*431_*435del
ENST00000607071.5:c.*1618+186_*1618+190del	ENSP00000475855.1:n.*1618+186_*1618+190del
ENST00000607742.5:c.*2962+186_*2962+190del	ENSP00000475523.1:n.*2962+186_*2962+190del
NM_032861.3:c.1684+186_1684+190del	NP_116250.3:n.1684+186_1684+190del
NR_073096.1:n.1803_1807del
XM_006715586.1:c.1474+186_1474+190del	XP_006715649.1:n.1474+186_1474+190del
XM_011536196.1:c.1663+186_1663+190del	XP_011534498.1:n.1663+186_1663+190del
XM_011536197.1:c.1570+186_1570+190del	XP_011534499.1:n.1570+186_1570+190del
XM_011536198.1:c.1474+186_1474+190del	XP_011534500.1:n.1474+186_1474+190del
XM_006715586.3:c.1474+186_1474+190del	XP_006715649.1:n.1474+186_1474+190del
XM_011536196.3:c.1663+186_1663+190del	XP_011534498.1:n.1663+186_1663+190del
XM_011536198.3:c.1474+186_1474+190del	XP_011534500.1:n.1474+186_1474+190del
XM_024446573.1:c.1684+186_1684+190del	XP_024302341.1:n.1684+186_1684+190del
XR_001743697.2:n.1715+186_1715+190del
XR_942606.2:n.1766+186_1766+190del
NM_032861.4:c.1684+186_1684+190del MANE Select	NP_116250.3:n.1684+186_1684+190del
NR_073096.2:n.1785_1789del