Canonical Allele Identifier: CA2680955726

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114570-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114573_158114574del , CM000668.2:g.158114573_158114574del	GRCh38
NC_000006.11:g.158535605_158535606del , CM000668.1:g.158535605_158535606del	GRCh37
NC_000006.10:g.158455593_158455594del	NCBI36
NG_032889.1:g.58709_58710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+217_*1404+218del	ENSP00000475855.1:n.*1404+217_*1404+218del
ENST00000642244.1:c.1594+217_1594+218del	ENSP00000493554.1:n.1594+217_1594+218del
ENST00000644972.1:c.1684+217_1684+218del	ENSP00000496451.1:n.1684+217_1684+218del
ENST00000645077.1:c.*1305+217_*1305+218del	ENSP00000496113.1:n.*1305+217_*1305+218del
ENST00000645172.1:c.*1386+217_*1386+218del	ENSP00000495367.1:n.*1386+217_*1386+218del
ENST00000646190.1:n.3015+217_3015+218del
ENST00000646208.1:c.1420+217_1420+218del	ENSP00000493723.1:n.1420+217_1420+218del
ENST00000646410.1:c.1555+217_1555+218del	ENSP00000494205.1:n.1555+217_1555+218del
ENST00000646562.1:c.*1735_*1736del	ENSP00000496087.1:n.*1735_*1736del
ENST00000647468.2:c.1684+217_1684+218del MANE Select	ENSP00000496731.1:n.1684+217_1684+218del
ENST00000648111.1:c.*1372+217_*1372+218del	ENSP00000497275.1:n.*1372+217_*1372+218del
ENST00000367104.7:c.1684+217_1684+218del	ENSP00000356071.3:n.1684+217_1684+218del
ENST00000606965.5:c.*462_*463del	ENSP00000475808.1:n.*462_*463del
ENST00000607071.5:c.*1618+217_*1618+218del	ENSP00000475855.1:n.*1618+217_*1618+218del
ENST00000607742.5:c.*2962+217_*2962+218del	ENSP00000475523.1:n.*2962+217_*2962+218del
NM_032861.3:c.1684+217_1684+218del	NP_116250.3:n.1684+217_1684+218del
NR_073096.1:n.1834_1835del
XM_006715586.1:c.1474+217_1474+218del	XP_006715649.1:n.1474+217_1474+218del
XM_011536196.1:c.1663+217_1663+218del	XP_011534498.1:n.1663+217_1663+218del
XM_011536197.1:c.1570+217_1570+218del	XP_011534499.1:n.1570+217_1570+218del
XM_011536198.1:c.1474+217_1474+218del	XP_011534500.1:n.1474+217_1474+218del
XM_006715586.3:c.1474+217_1474+218del	XP_006715649.1:n.1474+217_1474+218del
XM_011536196.3:c.1663+217_1663+218del	XP_011534498.1:n.1663+217_1663+218del
XM_011536198.3:c.1474+217_1474+218del	XP_011534500.1:n.1474+217_1474+218del
XM_024446573.1:c.1684+217_1684+218del	XP_024302341.1:n.1684+217_1684+218del
XR_001743697.2:n.1715+217_1715+218del
XR_942606.2:n.1766+217_1766+218del
NM_032861.4:c.1684+217_1684+218del MANE Select	NP_116250.3:n.1684+217_1684+218del
NR_073096.2:n.1816_1817del