Canonical Allele Identifier: CA1675959654

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115223_158115225delinsTCA , CM000668.2:g.158115223_158115225delinsTCA	GRCh38
NC_000006.11:g.158536255_158536257delinsTCA , CM000668.1:g.158536255_158536257delinsTCA	GRCh37
NC_000006.10:g.158456243_158456245delinsTCA	NCBI36
NG_032889.1:g.58056_58058delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-254_714-252delinsTGA	ENSP00000391168.2:n.714-254_714-252delinsTGA
ENST00000607071.6:c.*1222-254_*1222-252delinsTGA	ENSP00000475855.1:n.*1222-254_*1222-252delinsTGA
ENST00000642244.1:c.1412-254_1412-252delinsTGA	ENSP00000493554.1:n.1412-254_1412-252delinsTGA
ENST00000642903.1:c.1502-254_1502-252delinsTGA	ENSP00000493559.1:n.1502-254_1502-252delinsTGA
ENST00000644972.1:c.1502-254_1502-252delinsTGA	ENSP00000496451.1:n.1502-254_1502-252delinsTGA
ENST00000645077.1:c.*1123-254_*1123-252delinsTGA	ENSP00000496113.1:n.*1123-254_*1123-252delinsTGA
ENST00000645172.1:c.*1204-254_*1204-252delinsTGA	ENSP00000495367.1:n.*1204-254_*1204-252delinsTGA
ENST00000646190.1:n.2833-254_2833-252delinsTGA
ENST00000646208.1:c.1238-254_1238-252delinsTGA	ENSP00000493723.1:n.1238-254_1238-252delinsTGA
ENST00000646410.1:c.1373-254_1373-252delinsTGA	ENSP00000494205.1:n.1373-254_1373-252delinsTGA
ENST00000646562.1:c.*1336-254_*1336-252delinsTGA	ENSP00000496087.1:n.*1336-254_*1336-252delinsTGA
ENST00000647468.2:c.1502-254_1502-252delinsTGA MANE Select	ENSP00000496731.1:n.1502-254_1502-252delinsTGA
ENST00000648111.1:c.*1190-254_*1190-252delinsTGA	ENSP00000497275.1:n.*1190-254_*1190-252delinsTGA
ENST00000367101.5:c.1546-254_1546-252delinsTGA	ENSP00000356068.1:n.1546-254_1546-252delinsTGA
ENST00000367104.7:c.1502-254_1502-252delinsTGA	ENSP00000356071.3:n.1502-254_1502-252delinsTGA
ENST00000435180.5:c.227-254_227-252delinsTGA	ENSP00000391168.1:n.227-254_227-252delinsTGA
ENST00000606965.5:c.*63-254_*63-252delinsTGA	ENSP00000475808.1:n.*63-254_*63-252delinsTGA
ENST00000607071.5:c.*1436-254_*1436-252delinsTGA	ENSP00000475855.1:n.*1436-254_*1436-252delinsTGA
ENST00000607742.5:c.*2780-254_*2780-252delinsTGA	ENSP00000475523.1:n.*2780-254_*2780-252delinsTGA
NM_032861.3:c.1502-254_1502-252delinsTGA	NP_116250.3:n.1502-254_1502-252delinsTGA
NR_073096.1:n.1435-254_1435-252delinsTGA
XM_006715586.1:c.1292-254_1292-252delinsTGA	XP_006715649.1:n.1292-254_1292-252delinsTGA
XM_011536196.1:c.1481-254_1481-252delinsTGA	XP_011534498.1:n.1481-254_1481-252delinsTGA
XM_011536197.1:c.1388-254_1388-252delinsTGA	XP_011534499.1:n.1388-254_1388-252delinsTGA
XM_011536198.1:c.1292-254_1292-252delinsTGA	XP_011534500.1:n.1292-254_1292-252delinsTGA
XM_006715586.3:c.1292-254_1292-252delinsTGA	XP_006715649.1:n.1292-254_1292-252delinsTGA
XM_011536196.3:c.1481-254_1481-252delinsTGA	XP_011534498.1:n.1481-254_1481-252delinsTGA
XM_011536198.3:c.1292-254_1292-252delinsTGA	XP_011534500.1:n.1292-254_1292-252delinsTGA
XM_024446573.1:c.1502-254_1502-252delinsTGA	XP_024302341.1:n.1502-254_1502-252delinsTGA
XR_001743697.2:n.1533-254_1533-252delinsTGA
XR_942606.2:n.1584-254_1584-252delinsTGA
NM_032861.4:c.1502-254_1502-252delinsTGA MANE Select	NP_116250.3:n.1502-254_1502-252delinsTGA
NR_073096.2:n.1417-254_1417-252delinsTGA