Canonical Allele Identifier: CA2680956702

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114777-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114777_158114778insT , CM000668.2:g.158114777_158114778insT	GRCh38
NC_000006.11:g.158535809_158535810insT , CM000668.1:g.158535809_158535810insT	GRCh37
NC_000006.10:g.158455797_158455798insT	NCBI36
NG_032889.1:g.58503_58504insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+11_*1404+12insA	ENSP00000475855.1:n.*1404+11_*1404+12insA
ENST00000642244.1:c.1594+11_1594+12insA	ENSP00000493554.1:n.1594+11_1594+12insA
ENST00000642903.1:c.1695_1696insA	ENSP00000493559.1:p.Cys566MetfsTer3
ENST00000644972.1:c.1684+11_1684+12insA	ENSP00000496451.1:n.1684+11_1684+12insA
ENST00000645077.1:c.*1305+11_*1305+12insA	ENSP00000496113.1:n.*1305+11_*1305+12insA
ENST00000645172.1:c.*1386+11_*1386+12insA	ENSP00000495367.1:n.*1386+11_*1386+12insA
ENST00000646190.1:n.3015+11_3015+12insA
ENST00000646208.1:c.1420+11_1420+12insA	ENSP00000493723.1:n.1420+11_1420+12insA
ENST00000646410.1:c.1555+11_1555+12insA	ENSP00000494205.1:n.1555+11_1555+12insA
ENST00000646562.1:c.*1529_*1530insA	ENSP00000496087.1:n.*1529_*1530insA
ENST00000647468.2:c.1684+11_1684+12insA MANE Select	ENSP00000496731.1:n.1684+11_1684+12insA
ENST00000648111.1:c.*1372+11_*1372+12insA	ENSP00000497275.1:n.*1372+11_*1372+12insA
ENST00000367101.5:c.*143_*144insA	ENSP00000356068.1:n.*143_*144insA
ENST00000367104.7:c.1684+11_1684+12insA	ENSP00000356071.3:n.1684+11_1684+12insA
ENST00000435180.5:c.420_421insA	ENSP00000391168.1:p.Cys141MetfsTer3
ENST00000606965.5:c.*256_*257insA	ENSP00000475808.1:n.*256_*257insA
ENST00000607071.5:c.*1618+11_*1618+12insA	ENSP00000475855.1:n.*1618+11_*1618+12insA
ENST00000607742.5:c.*2962+11_*2962+12insA	ENSP00000475523.1:n.*2962+11_*2962+12insA
NM_032861.3:c.1684+11_1684+12insA	NP_116250.3:n.1684+11_1684+12insA
NR_073096.1:n.1628_1629insA
XM_006715586.1:c.1474+11_1474+12insA	XP_006715649.1:n.1474+11_1474+12insA
XM_011536196.1:c.1663+11_1663+12insA	XP_011534498.1:n.1663+11_1663+12insA
XM_011536197.1:c.1570+11_1570+12insA	XP_011534499.1:n.1570+11_1570+12insA
XM_011536198.1:c.1474+11_1474+12insA	XP_011534500.1:n.1474+11_1474+12insA
XM_006715586.3:c.1474+11_1474+12insA	XP_006715649.1:n.1474+11_1474+12insA
XM_011536196.3:c.1663+11_1663+12insA	XP_011534498.1:n.1663+11_1663+12insA
XM_011536198.3:c.1474+11_1474+12insA	XP_011534500.1:n.1474+11_1474+12insA
XM_024446573.1:c.1684+11_1684+12insA	XP_024302341.1:n.1684+11_1684+12insA
XR_001743697.2:n.1715+11_1715+12insA
XR_942606.2:n.1766+11_1766+12insA
NM_032861.4:c.1684+11_1684+12insA MANE Select	NP_116250.3:n.1684+11_1684+12insA
NR_073096.2:n.1610_1611insA