Canonical Allele Identifier: CA2680956969

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158115107-TCTGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158115109_158115113del , CM000668.2:g.158115109_158115113del	GRCh38
NC_000006.11:g.158536141_158536145del , CM000668.1:g.158536141_158536145del	GRCh37
NC_000006.10:g.158456129_158456133del	NCBI36
NG_032889.1:g.58169_58173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.714-141_714-137del	ENSP00000391168.2:n.714-141_714-137del
ENST00000607071.6:c.*1222-141_*1222-137del	ENSP00000475855.1:n.*1222-141_*1222-137del
ENST00000642244.1:c.1412-141_1412-137del	ENSP00000493554.1:n.1412-141_1412-137del
ENST00000642903.1:c.1502-141_1502-137del	ENSP00000493559.1:n.1502-141_1502-137del
ENST00000644972.1:c.1502-141_1502-137del	ENSP00000496451.1:n.1502-141_1502-137del
ENST00000645077.1:c.*1123-141_*1123-137del	ENSP00000496113.1:n.*1123-141_*1123-137del
ENST00000645172.1:c.*1204-141_*1204-137del	ENSP00000495367.1:n.*1204-141_*1204-137del
ENST00000646190.1:n.2833-141_2833-137del
ENST00000646208.1:c.1238-141_1238-137del	ENSP00000493723.1:n.1238-141_1238-137del
ENST00000646410.1:c.1373-141_1373-137del	ENSP00000494205.1:n.1373-141_1373-137del
ENST00000646562.1:c.*1336-141_*1336-137del	ENSP00000496087.1:n.*1336-141_*1336-137del
ENST00000647468.2:c.1502-141_1502-137del MANE Select	ENSP00000496731.1:n.1502-141_1502-137del
ENST00000648111.1:c.*1190-141_*1190-137del	ENSP00000497275.1:n.*1190-141_*1190-137del
ENST00000367101.5:c.1546-141_1546-137del	ENSP00000356068.1:n.1546-141_1546-137del
ENST00000367104.7:c.1502-141_1502-137del	ENSP00000356071.3:n.1502-141_1502-137del
ENST00000435180.5:c.227-141_227-137del	ENSP00000391168.1:n.227-141_227-137del
ENST00000606965.5:c.*63-141_*63-137del	ENSP00000475808.1:n.*63-141_*63-137del
ENST00000607071.5:c.*1436-141_*1436-137del	ENSP00000475855.1:n.*1436-141_*1436-137del
ENST00000607742.5:c.*2780-141_*2780-137del	ENSP00000475523.1:n.*2780-141_*2780-137del
NM_032861.3:c.1502-141_1502-137del	NP_116250.3:n.1502-141_1502-137del
NR_073096.1:n.1435-141_1435-137del
XM_006715586.1:c.1292-141_1292-137del	XP_006715649.1:n.1292-141_1292-137del
XM_011536196.1:c.1481-141_1481-137del	XP_011534498.1:n.1481-141_1481-137del
XM_011536197.1:c.1388-141_1388-137del	XP_011534499.1:n.1388-141_1388-137del
XM_011536198.1:c.1292-141_1292-137del	XP_011534500.1:n.1292-141_1292-137del
XM_006715586.3:c.1292-141_1292-137del	XP_006715649.1:n.1292-141_1292-137del
XM_011536196.3:c.1481-141_1481-137del	XP_011534498.1:n.1481-141_1481-137del
XM_011536198.3:c.1292-141_1292-137del	XP_011534500.1:n.1292-141_1292-137del
XM_024446573.1:c.1502-141_1502-137del	XP_024302341.1:n.1502-141_1502-137del
XR_001743697.2:n.1533-141_1533-137del
XR_942606.2:n.1584-141_1584-137del
NM_032861.4:c.1502-141_1502-137del MANE Select	NP_116250.3:n.1502-141_1502-137del
NR_073096.2:n.1417-141_1417-137del