Canonical Allele Identifier: CA821386221

Gene: SERAC1

Linked Data

• dbSNP Id: rs1471275627
• gnomAD v3: 6-158114627-AAAG-A
• gnomAD v4: 6-158114627-AAAG-A
• MyVariant Identifiers: chr6:g.158535660_158535662del (hg19) ; chr6:g.158114628_158114630del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114630_158114632del , CM000668.2:g.158114630_158114632del	GRCh38
NC_000006.11:g.158535662_158535664del , CM000668.1:g.158535662_158535664del	GRCh37
NC_000006.10:g.158455650_158455652del	NCBI36
NG_032889.1:g.58651_58653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+159_*1404+161del	ENSP00000475855.1:n.*1404+159_*1404+161del
ENST00000642244.1:c.1594+159_1594+161del	ENSP00000493554.1:n.1594+159_1594+161del
ENST00000642903.1:c.*79_*81del	ENSP00000493559.1:n.*79_*81del
ENST00000644972.1:c.1684+159_1684+161del	ENSP00000496451.1:n.1684+159_1684+161del
ENST00000645077.1:c.*1305+159_*1305+161del	ENSP00000496113.1:n.*1305+159_*1305+161del
ENST00000645172.1:c.*1386+159_*1386+161del	ENSP00000495367.1:n.*1386+159_*1386+161del
ENST00000646190.1:n.3015+159_3015+161del
ENST00000646208.1:c.1420+159_1420+161del	ENSP00000493723.1:n.1420+159_1420+161del
ENST00000646410.1:c.1555+159_1555+161del	ENSP00000494205.1:n.1555+159_1555+161del
ENST00000646562.1:c.*1677_*1679del	ENSP00000496087.1:n.*1677_*1679del
ENST00000647468.2:c.1684+159_1684+161del MANE Select	ENSP00000496731.1:n.1684+159_1684+161del
ENST00000648111.1:c.*1372+159_*1372+161del	ENSP00000497275.1:n.*1372+159_*1372+161del
ENST00000367104.7:c.1684+159_1684+161del	ENSP00000356071.3:n.1684+159_1684+161del
ENST00000606965.5:c.*404_*406del	ENSP00000475808.1:n.*404_*406del
ENST00000607071.5:c.*1618+159_*1618+161del	ENSP00000475855.1:n.*1618+159_*1618+161del
ENST00000607742.5:c.*2962+159_*2962+161del	ENSP00000475523.1:n.*2962+159_*2962+161del
NM_032861.3:c.1684+159_1684+161del	NP_116250.3:n.1684+159_1684+161del
NR_073096.1:n.1776_1778del
XM_006715586.1:c.1474+159_1474+161del	XP_006715649.1:n.1474+159_1474+161del
XM_011536196.1:c.1663+159_1663+161del	XP_011534498.1:n.1663+159_1663+161del
XM_011536197.1:c.1570+159_1570+161del	XP_011534499.1:n.1570+159_1570+161del
XM_011536198.1:c.1474+159_1474+161del	XP_011534500.1:n.1474+159_1474+161del
XM_006715586.3:c.1474+159_1474+161del	XP_006715649.1:n.1474+159_1474+161del
XM_011536196.3:c.1663+159_1663+161del	XP_011534498.1:n.1663+159_1663+161del
XM_011536198.3:c.1474+159_1474+161del	XP_011534500.1:n.1474+159_1474+161del
XM_024446573.1:c.1684+159_1684+161del	XP_024302341.1:n.1684+159_1684+161del
XR_001743697.2:n.1715+159_1715+161del
XR_942606.2:n.1766+159_1766+161del
NM_032861.4:c.1684+159_1684+161del MANE Select	NP_116250.3:n.1684+159_1684+161del
NR_073096.2:n.1758_1760del