Canonical Allele Identifier: CA1096370143

Gene: SERAC1

Linked Data

• dbSNP Id: rs1784232644
• gnomAD v3: 6-158114640-GCCCAA-G
• gnomAD v4: 6-158114640-GCCCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114646_158114650del , CM000668.2:g.158114646_158114650del	GRCh38
NC_000006.11:g.158535678_158535682del , CM000668.1:g.158535678_158535682del	GRCh37
NC_000006.10:g.158455666_158455670del	NCBI36
NG_032889.1:g.58636_58640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+144_*1404+148del	ENSP00000475855.1:n.*1404+144_*1404+148del
ENST00000642244.1:c.1594+144_1594+148del	ENSP00000493554.1:n.1594+144_1594+148del
ENST00000642903.1:c.*64_*68del	ENSP00000493559.1:n.*64_*68del
ENST00000644972.1:c.1684+144_1684+148del	ENSP00000496451.1:n.1684+144_1684+148del
ENST00000645077.1:c.*1305+144_*1305+148del	ENSP00000496113.1:n.*1305+144_*1305+148del
ENST00000645172.1:c.*1386+144_*1386+148del	ENSP00000495367.1:n.*1386+144_*1386+148del
ENST00000646190.1:n.3015+144_3015+148del
ENST00000646208.1:c.1420+144_1420+148del	ENSP00000493723.1:n.1420+144_1420+148del
ENST00000646410.1:c.1555+144_1555+148del	ENSP00000494205.1:n.1555+144_1555+148del
ENST00000646562.1:c.*1662_*1666del	ENSP00000496087.1:n.*1662_*1666del
ENST00000647468.2:c.1684+144_1684+148del MANE Select	ENSP00000496731.1:n.1684+144_1684+148del
ENST00000648111.1:c.*1372+144_*1372+148del	ENSP00000497275.1:n.*1372+144_*1372+148del
ENST00000367104.7:c.1684+144_1684+148del	ENSP00000356071.3:n.1684+144_1684+148del
ENST00000606965.5:c.*389_*393del	ENSP00000475808.1:n.*389_*393del
ENST00000607071.5:c.*1618+144_*1618+148del	ENSP00000475855.1:n.*1618+144_*1618+148del
ENST00000607742.5:c.*2962+144_*2962+148del	ENSP00000475523.1:n.*2962+144_*2962+148del
NM_032861.3:c.1684+144_1684+148del	NP_116250.3:n.1684+144_1684+148del
NR_073096.1:n.1761_1765del
XM_006715586.1:c.1474+144_1474+148del	XP_006715649.1:n.1474+144_1474+148del
XM_011536196.1:c.1663+144_1663+148del	XP_011534498.1:n.1663+144_1663+148del
XM_011536197.1:c.1570+144_1570+148del	XP_011534499.1:n.1570+144_1570+148del
XM_011536198.1:c.1474+144_1474+148del	XP_011534500.1:n.1474+144_1474+148del
XM_006715586.3:c.1474+144_1474+148del	XP_006715649.1:n.1474+144_1474+148del
XM_011536196.3:c.1663+144_1663+148del	XP_011534498.1:n.1663+144_1663+148del
XM_011536198.3:c.1474+144_1474+148del	XP_011534500.1:n.1474+144_1474+148del
XM_024446573.1:c.1684+144_1684+148del	XP_024302341.1:n.1684+144_1684+148del
XR_001743697.2:n.1715+144_1715+148del
XR_942606.2:n.1766+144_1766+148del
NM_032861.4:c.1684+144_1684+148del MANE Select	NP_116250.3:n.1684+144_1684+148del
NR_073096.2:n.1743_1747del