Canonical Allele Identifier: CA1675959437

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114868A= , CM000668.2:g.158114868A=	GRCh38
NC_000006.11:g.158535900A= , CM000668.1:g.158535900A=	GRCh37
NC_000006.10:g.158455888A=	NCBI36
NG_032889.1:g.58413T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.817T=	ENSP00000391168.2:n.817T=
ENST00000607071.6:c.*1325T=	ENSP00000475855.1:n.*1325T=
ENST00000642244.1:c.1515T=	ENSP00000493554.1:p.His505=
ENST00000642903.1:c.1605T=	ENSP00000493559.1:p.His535=
ENST00000644972.1:c.1605T=	ENSP00000496451.1:p.His535=
ENST00000645077.1:c.*1226T=	ENSP00000496113.1:n.*1226T=
ENST00000645172.1:c.*1307T=	ENSP00000495367.1:n.*1307T=
ENST00000646190.1:n.2936T=
ENST00000646208.1:c.1341T=	ENSP00000493723.1:p.His447=
ENST00000646410.1:c.1476T=	ENSP00000494205.1:p.His492=
ENST00000646562.1:c.*1439T=	ENSP00000496087.1:n.*1439T=
ENST00000647468.2:c.1605T= MANE Select	ENSP00000496731.1:p.His535=
ENST00000648111.1:c.*1293T=	ENSP00000497275.1:n.*1293T=
ENST00000367101.5:c.*53T=	ENSP00000356068.1:n.*53T=
ENST00000367104.7:c.1605T=	ENSP00000356071.3:p.His535=
ENST00000435180.5:c.330T=	ENSP00000391168.1:p.His110=
ENST00000606965.5:c.*166T=	ENSP00000475808.1:n.*166T=
ENST00000607071.5:c.*1539T=	ENSP00000475855.1:n.*1539T=
ENST00000607742.5:c.*2883T=	ENSP00000475523.1:n.*2883T=
NM_032861.3:c.1605T=	NP_116250.3:p.His535=
NR_073096.1:n.1538T=
XM_006715586.1:c.1395T=	XP_006715649.1:p.His465=
XM_011536196.1:c.1584T=	XP_011534498.1:p.His528=
XM_011536197.1:c.1491T=	XP_011534499.1:p.His497=
XM_011536198.1:c.1395T=	XP_011534500.1:p.His465=
XM_006715586.3:c.1395T=	XP_006715649.1:p.His465=
XM_011536196.3:c.1584T=	XP_011534498.1:p.His528=
XM_011536198.3:c.1395T=	XP_011534500.1:p.His465=
XM_024446573.1:c.1605T=	XP_024302341.1:p.His535=
XR_001743697.2:n.1636T=
XR_942606.2:n.1687T=
NM_032861.4:c.1605T= MANE Select	NP_116250.3:p.His535=
NR_073096.2:n.1520T=