Canonical Allele Identifier: CA1675978270

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146830_158146831delinsTG , CM000668.2:g.158146830_158146831delinsTG	GRCh38
NC_000006.11:g.158567862_158567863delinsTG , CM000668.1:g.158567862_158567863delinsTG	GRCh37
NC_000006.10:g.158487850_158487851delinsTG	NCBI36
NG_032889.1:g.26450_26451delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*272_*273delinsCA	ENSP00000475855.1:n.*272_*273delinsCA
ENST00000642244.1:c.348_349delinsCA	ENSP00000493554.1:p.Thr116=
ENST00000642903.1:c.438_439delinsCA	ENSP00000493559.1:p.Thr146=
ENST00000644972.1:c.438_439delinsCA	ENSP00000496451.1:p.Thr146=
ENST00000645077.1:c.*272_*273delinsCA	ENSP00000496113.1:n.*272_*273delinsCA
ENST00000645172.1:c.*189+2034_*189+2035delinsCA	ENSP00000495367.1:n.*189+2034_*189+2035delinsCA
ENST00000646190.1:n.1669_1670delinsCA
ENST00000646208.1:c.174_175delinsCA	ENSP00000493723.1:p.Thr58=
ENST00000646410.1:c.309_310delinsCA	ENSP00000494205.1:p.Thr103=
ENST00000646562.1:c.*272_*273delinsCA	ENSP00000496087.1:n.*272_*273delinsCA
ENST00000647468.2:c.438_439delinsCA MANE Select	ENSP00000496731.1:p.Thr146=
ENST00000648111.1:c.*82_*83delinsCA	ENSP00000497275.1:n.*82_*83delinsCA
ENST00000367101.5:c.438_439delinsCA	ENSP00000356068.1:p.Thr146=
ENST00000367104.7:c.438_439delinsCA	ENSP00000356071.3:p.Thr146=
ENST00000606965.5:c.438_439delinsCA	ENSP00000475808.1:p.Thr146=
ENST00000607000.1:c.438_439delinsCA	ENSP00000475788.1:p.Thr146=
ENST00000607071.5:c.*272_*273delinsCA	ENSP00000475855.1:n.*272_*273delinsCA
ENST00000607742.5:c.*272_*273delinsCA	ENSP00000475523.1:n.*272_*273delinsCA
NM_032861.3:c.438_439delinsCA	NP_116250.3:p.Thr146=
NR_073096.1:n.580_581delinsCA
XM_006715586.1:c.228_229delinsCA	XP_006715649.1:p.Thr76=
XM_011536196.1:c.417_418delinsCA	XP_011534498.1:p.Thr139=
XM_011536197.1:c.438_439delinsCA	XP_011534499.1:p.Thr146=
XM_011536198.1:c.228_229delinsCA	XP_011534500.1:p.Thr76=
XR_942606.1:n.439_440delinsCA
XM_006715586.3:c.228_229delinsCA	XP_006715649.1:p.Thr76=
XM_011536196.3:c.417_418delinsCA	XP_011534498.1:p.Thr139=
XM_011536198.3:c.228_229delinsCA	XP_011534500.1:p.Thr76=
XM_024446573.1:c.438_439delinsCA	XP_024302341.1:p.Thr146=
XR_001743697.2:n.519_520delinsCA
XR_942606.2:n.570_571delinsCA
NM_032861.4:c.438_439delinsCA MANE Select	NP_116250.3:p.Thr146=
NR_073096.2:n.562_563delinsCA