Canonical Allele Identifier: CA2680955739

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114596-T-TAATGGCTTAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114597_158114606dup , CM000668.2:g.158114597_158114606dup	GRCh38
NC_000006.11:g.158535629_158535638dup , CM000668.1:g.158535629_158535638dup	GRCh37
NC_000006.10:g.158455617_158455626dup	NCBI36
NG_032889.1:g.58675_58684dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+183_*1404+192dup	ENSP00000475855.1:n.*1404+183_*1404+192dup
ENST00000642244.1:c.1594+183_1594+192dup	ENSP00000493554.1:n.1594+183_1594+192dup
ENST00000642903.1:c.*103_*112dup	ENSP00000493559.1:n.*103_*112dup
ENST00000644972.1:c.1684+183_1684+192dup	ENSP00000496451.1:n.1684+183_1684+192dup
ENST00000645077.1:c.*1305+183_*1305+192dup	ENSP00000496113.1:n.*1305+183_*1305+192dup
ENST00000645172.1:c.*1386+183_*1386+192dup	ENSP00000495367.1:n.*1386+183_*1386+192dup
ENST00000646190.1:n.3015+183_3015+192dup
ENST00000646208.1:c.1420+183_1420+192dup	ENSP00000493723.1:n.1420+183_1420+192dup
ENST00000646410.1:c.1555+183_1555+192dup	ENSP00000494205.1:n.1555+183_1555+192dup
ENST00000646562.1:c.*1701_*1710dup	ENSP00000496087.1:n.*1701_*1710dup
ENST00000647468.2:c.1684+183_1684+192dup MANE Select	ENSP00000496731.1:n.1684+183_1684+192dup
ENST00000648111.1:c.*1372+183_*1372+192dup	ENSP00000497275.1:n.*1372+183_*1372+192dup
ENST00000367104.7:c.1684+183_1684+192dup	ENSP00000356071.3:n.1684+183_1684+192dup
ENST00000606965.5:c.*428_*437dup	ENSP00000475808.1:n.*428_*437dup
ENST00000607071.5:c.*1618+183_*1618+192dup	ENSP00000475855.1:n.*1618+183_*1618+192dup
ENST00000607742.5:c.*2962+183_*2962+192dup	ENSP00000475523.1:n.*2962+183_*2962+192dup
NM_032861.3:c.1684+183_1684+192dup	NP_116250.3:n.1684+183_1684+192dup
NR_073096.1:n.1800_1809dup
XM_006715586.1:c.1474+183_1474+192dup	XP_006715649.1:n.1474+183_1474+192dup
XM_011536196.1:c.1663+183_1663+192dup	XP_011534498.1:n.1663+183_1663+192dup
XM_011536197.1:c.1570+183_1570+192dup	XP_011534499.1:n.1570+183_1570+192dup
XM_011536198.1:c.1474+183_1474+192dup	XP_011534500.1:n.1474+183_1474+192dup
XM_006715586.3:c.1474+183_1474+192dup	XP_006715649.1:n.1474+183_1474+192dup
XM_011536196.3:c.1663+183_1663+192dup	XP_011534498.1:n.1663+183_1663+192dup
XM_011536198.3:c.1474+183_1474+192dup	XP_011534500.1:n.1474+183_1474+192dup
XM_024446573.1:c.1684+183_1684+192dup	XP_024302341.1:n.1684+183_1684+192dup
XR_001743697.2:n.1715+183_1715+192dup
XR_942606.2:n.1766+183_1766+192dup
NM_032861.4:c.1684+183_1684+192dup MANE Select	NP_116250.3:n.1684+183_1684+192dup
NR_073096.2:n.1782_1791dup