Canonical Allele Identifier: CA2773733427

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115037_158115038insGGG , CM000668.2:g.158115037_158115038insGGG	GRCh38
NC_000006.11:g.158536069_158536070insGGG , CM000668.1:g.158536069_158536070insGGG	GRCh37
NC_000006.10:g.158456057_158456058insGGG	NCBI36
NG_032889.1:g.58243_58244insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-67_714-66insCCC	ENSP00000391168.2:n.714-67_714-66insCCC
ENST00000607071.6:c.*1222-67_*1222-66insCCC	ENSP00000475855.1:n.*1222-67_*1222-66insCCC
ENST00000642244.1:c.1412-67_1412-66insCCC	ENSP00000493554.1:n.1412-67_1412-66insCCC
ENST00000642903.1:c.1502-67_1502-66insCCC	ENSP00000493559.1:n.1502-67_1502-66insCCC
ENST00000644972.1:c.1502-67_1502-66insCCC	ENSP00000496451.1:n.1502-67_1502-66insCCC
ENST00000645077.1:c.*1123-67_*1123-66insCCC	ENSP00000496113.1:n.*1123-67_*1123-66insCCC
ENST00000645172.1:c.*1204-67_*1204-66insCCC	ENSP00000495367.1:n.*1204-67_*1204-66insCCC
ENST00000646190.1:n.2833-67_2833-66insCCC
ENST00000646208.1:c.1238-67_1238-66insCCC	ENSP00000493723.1:n.1238-67_1238-66insCCC
ENST00000646410.1:c.1373-67_1373-66insCCC	ENSP00000494205.1:n.1373-67_1373-66insCCC
ENST00000646562.1:c.*1336-67_*1336-66insCCC	ENSP00000496087.1:n.*1336-67_*1336-66insCCC
ENST00000647468.2:c.1502-67_1502-66insCCC MANE Select	ENSP00000496731.1:n.1502-67_1502-66insCCC
ENST00000648111.1:c.*1190-67_*1190-66insCCC	ENSP00000497275.1:n.*1190-67_*1190-66insCCC
ENST00000367101.5:c.1546-67_1546-66insCCC	ENSP00000356068.1:n.1546-67_1546-66insCCC
ENST00000367104.7:c.1502-67_1502-66insCCC	ENSP00000356071.3:n.1502-67_1502-66insCCC
ENST00000435180.5:c.227-67_227-66insCCC	ENSP00000391168.1:n.227-67_227-66insCCC
ENST00000606965.5:c.*63-67_*63-66insCCC	ENSP00000475808.1:n.*63-67_*63-66insCCC
ENST00000607071.5:c.*1436-67_*1436-66insCCC	ENSP00000475855.1:n.*1436-67_*1436-66insCCC
ENST00000607742.5:c.*2780-67_*2780-66insCCC	ENSP00000475523.1:n.*2780-67_*2780-66insCCC
NM_032861.3:c.1502-67_1502-66insCCC	NP_116250.3:n.1502-67_1502-66insCCC
NR_073096.1:n.1435-67_1435-66insCCC
XM_006715586.1:c.1292-67_1292-66insCCC	XP_006715649.1:n.1292-67_1292-66insCCC
XM_011536196.1:c.1481-67_1481-66insCCC	XP_011534498.1:n.1481-67_1481-66insCCC
XM_011536197.1:c.1388-67_1388-66insCCC	XP_011534499.1:n.1388-67_1388-66insCCC
XM_011536198.1:c.1292-67_1292-66insCCC	XP_011534500.1:n.1292-67_1292-66insCCC
XM_006715586.3:c.1292-67_1292-66insCCC	XP_006715649.1:n.1292-67_1292-66insCCC
XM_011536196.3:c.1481-67_1481-66insCCC	XP_011534498.1:n.1481-67_1481-66insCCC
XM_011536198.3:c.1292-67_1292-66insCCC	XP_011534500.1:n.1292-67_1292-66insCCC
XM_024446573.1:c.1502-67_1502-66insCCC	XP_024302341.1:n.1502-67_1502-66insCCC
XR_001743697.2:n.1533-67_1533-66insCCC
XR_942606.2:n.1584-67_1584-66insCCC
NM_032861.4:c.1502-67_1502-66insCCC MANE Select	NP_116250.3:n.1502-67_1502-66insCCC
NR_073096.2:n.1417-67_1417-66insCCC