Canonical Allele Identifier: CA2680956767

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114884-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114890del , CM000668.2:g.158114890del	GRCh38
NC_000006.11:g.158535922del , CM000668.1:g.158535922del	GRCh37
NC_000006.10:g.158455910del	NCBI36
NG_032889.1:g.58396del

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.800del	ENSP00000391168.2:n.800del
ENST00000607071.6:c.*1308del	ENSP00000475855.1:n.*1308del
ENST00000642244.1:c.1498del	ENSP00000493554.1:p.Tyr500IlefsTer?
ENST00000642903.1:c.1588del	ENSP00000493559.1:p.Tyr530IlefsTer?
ENST00000644972.1:c.1588del	ENSP00000496451.1:p.Tyr530IlefsTer?
ENST00000645077.1:c.*1209del	ENSP00000496113.1:n.*1209del
ENST00000645172.1:c.*1290del	ENSP00000495367.1:n.*1290del
ENST00000646190.1:n.2919del
ENST00000646208.1:c.1324del	ENSP00000493723.1:p.Tyr442IlefsTer?
ENST00000646410.1:c.1459del	ENSP00000494205.1:p.Tyr487IlefsTer?
ENST00000646562.1:c.*1422del	ENSP00000496087.1:n.*1422del
ENST00000647468.2:c.1588del MANE Select	ENSP00000496731.1:p.Tyr530IlefsTer?
ENST00000648111.1:c.*1276del	ENSP00000497275.1:n.*1276del
ENST00000367101.5:c.*36del	ENSP00000356068.1:n.*36del
ENST00000367104.7:c.1588del	ENSP00000356071.3:p.Tyr530IlefsTer?
ENST00000435180.5:c.313del	ENSP00000391168.1:p.Tyr105IlefsTer?
ENST00000606965.5:c.*149del	ENSP00000475808.1:n.*149del
ENST00000607071.5:c.*1522del	ENSP00000475855.1:n.*1522del
ENST00000607742.5:c.*2866del	ENSP00000475523.1:n.*2866del
NM_032861.3:c.1588del	NP_116250.3:p.Tyr530IlefsTer?
NR_073096.1:n.1521del
XM_006715586.1:c.1378del	XP_006715649.1:p.Tyr460IlefsTer?
XM_011536196.1:c.1567del	XP_011534498.1:p.Tyr523IlefsTer?
XM_011536197.1:c.1474del	XP_011534499.1:p.Tyr492IlefsTer?
XM_011536198.1:c.1378del	XP_011534500.1:p.Tyr460IlefsTer?
XM_006715586.3:c.1378del	XP_006715649.1:p.Tyr460IlefsTer?
XM_011536196.3:c.1567del	XP_011534498.1:p.Tyr523IlefsTer?
XM_011536198.3:c.1378del	XP_011534500.1:p.Tyr460IlefsTer?
XM_024446573.1:c.1588del	XP_024302341.1:p.Tyr530IlefsTer?
XR_001743697.2:n.1619del
XR_942606.2:n.1670del
NM_032861.4:c.1588del MANE Select	NP_116250.3:p.Tyr530IlefsTer?
NR_073096.2:n.1503del