Canonical Allele Identifier: CA150915546

Gene: SERAC1

Linked Data

• ClinVar Variation Id: 1212700
• ClinVar RCV Id: RCV001586347
• dbSNP Id: rs200884183
• gnomAD v2: 6-158536218-G-GTAA
• gnomAD v3: 6-158115186-G-GTAA
• gnomAD v4: 6-158115186-G-GTAA
• MyVariant Identifiers: chr6:g.158536218_158536219insTAA (hg19) ; chr6:g.158115186_158115187insTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115186_158115187insTAA , CM000668.2:g.158115186_158115187insTAA	GRCh38
NC_000006.11:g.158536218_158536219insTAA , CM000668.1:g.158536218_158536219insTAA	GRCh37
NC_000006.10:g.158456206_158456207insTAA	NCBI36
NG_032889.1:g.58094_58095insTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-216_714-215insTTA	ENSP00000391168.2:n.714-216_714-215insTTA
ENST00000607071.6:c.*1222-216_*1222-215insTTA	ENSP00000475855.1:n.*1222-216_*1222-215insTTA
ENST00000642244.1:c.1412-216_1412-215insTTA	ENSP00000493554.1:n.1412-216_1412-215insTTA
ENST00000642903.1:c.1502-216_1502-215insTTA	ENSP00000493559.1:n.1502-216_1502-215insTTA
ENST00000644972.1:c.1502-216_1502-215insTTA	ENSP00000496451.1:n.1502-216_1502-215insTTA
ENST00000645077.1:c.*1123-216_*1123-215insTTA	ENSP00000496113.1:n.*1123-216_*1123-215insTTA
ENST00000645172.1:c.*1204-216_*1204-215insTTA	ENSP00000495367.1:n.*1204-216_*1204-215insTTA
ENST00000646190.1:n.2833-216_2833-215insTTA
ENST00000646208.1:c.1238-216_1238-215insTTA	ENSP00000493723.1:n.1238-216_1238-215insTTA
ENST00000646410.1:c.1373-216_1373-215insTTA	ENSP00000494205.1:n.1373-216_1373-215insTTA
ENST00000646562.1:c.*1336-216_*1336-215insTTA	ENSP00000496087.1:n.*1336-216_*1336-215insTTA
ENST00000647468.2:c.1502-216_1502-215insTTA MANE Select	ENSP00000496731.1:n.1502-216_1502-215insTTA
ENST00000648111.1:c.*1190-216_*1190-215insTTA	ENSP00000497275.1:n.*1190-216_*1190-215insTTA
ENST00000367101.5:c.1546-216_1546-215insTTA	ENSP00000356068.1:n.1546-216_1546-215insTTA
ENST00000367104.7:c.1502-216_1502-215insTTA	ENSP00000356071.3:n.1502-216_1502-215insTTA
ENST00000435180.5:c.227-216_227-215insTTA	ENSP00000391168.1:n.227-216_227-215insTTA
ENST00000606965.5:c.*63-216_*63-215insTTA	ENSP00000475808.1:n.*63-216_*63-215insTTA
ENST00000607071.5:c.*1436-216_*1436-215insTTA	ENSP00000475855.1:n.*1436-216_*1436-215insTTA
ENST00000607742.5:c.*2780-216_*2780-215insTTA	ENSP00000475523.1:n.*2780-216_*2780-215insTTA
NM_032861.3:c.1502-216_1502-215insTTA	NP_116250.3:n.1502-216_1502-215insTTA
NR_073096.1:n.1435-216_1435-215insTTA
XM_006715586.1:c.1292-216_1292-215insTTA	XP_006715649.1:n.1292-216_1292-215insTTA
XM_011536196.1:c.1481-216_1481-215insTTA	XP_011534498.1:n.1481-216_1481-215insTTA
XM_011536197.1:c.1388-216_1388-215insTTA	XP_011534499.1:n.1388-216_1388-215insTTA
XM_011536198.1:c.1292-216_1292-215insTTA	XP_011534500.1:n.1292-216_1292-215insTTA
XM_006715586.3:c.1292-216_1292-215insTTA	XP_006715649.1:n.1292-216_1292-215insTTA
XM_011536196.3:c.1481-216_1481-215insTTA	XP_011534498.1:n.1481-216_1481-215insTTA
XM_011536198.3:c.1292-216_1292-215insTTA	XP_011534500.1:n.1292-216_1292-215insTTA
XM_024446573.1:c.1502-216_1502-215insTTA	XP_024302341.1:n.1502-216_1502-215insTTA
XR_001743697.2:n.1533-216_1533-215insTTA
XR_942606.2:n.1584-216_1584-215insTTA
NM_032861.4:c.1502-216_1502-215insTTA MANE Select	NP_116250.3:n.1502-216_1502-215insTTA
NR_073096.2:n.1417-216_1417-215insTTA