Canonical Allele Identifier: CA1675959179

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114700A= , CM000668.2:g.158114700A=	GRCh38
NC_000006.11:g.158535732A= , CM000668.1:g.158535732A=	GRCh37
NC_000006.10:g.158455720A=	NCBI36
NG_032889.1:g.58581T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+89T=	ENSP00000475855.1:n.*1404+89T=
ENST00000642244.1:c.1594+89T=	ENSP00000493554.1:n.1594+89T=
ENST00000642903.1:c.*9T=	ENSP00000493559.1:n.*9T=
ENST00000644972.1:c.1684+89T=	ENSP00000496451.1:n.1684+89T=
ENST00000645077.1:c.*1305+89T=	ENSP00000496113.1:n.*1305+89T=
ENST00000645172.1:c.*1386+89T=	ENSP00000495367.1:n.*1386+89T=
ENST00000646190.1:n.3015+89T=
ENST00000646208.1:c.1420+89T=	ENSP00000493723.1:n.1420+89T=
ENST00000646410.1:c.1555+89T=	ENSP00000494205.1:n.1555+89T=
ENST00000646562.1:c.*1607T=	ENSP00000496087.1:n.*1607T=
ENST00000647468.2:c.1684+89T= MANE Select	ENSP00000496731.1:n.1684+89T=
ENST00000648111.1:c.*1372+89T=	ENSP00000497275.1:n.*1372+89T=
ENST00000367104.7:c.1684+89T=	ENSP00000356071.3:n.1684+89T=
ENST00000435180.5:c.498T=	ENSP00000391168.1:n.498T=
ENST00000606965.5:c.*334T=	ENSP00000475808.1:n.*334T=
ENST00000607071.5:c.*1618+89T=	ENSP00000475855.1:n.*1618+89T=
ENST00000607742.5:c.*2962+89T=	ENSP00000475523.1:n.*2962+89T=
NM_032861.3:c.1684+89T=	NP_116250.3:n.1684+89T=
NR_073096.1:n.1706T=
XM_006715586.1:c.1474+89T=	XP_006715649.1:n.1474+89T=
XM_011536196.1:c.1663+89T=	XP_011534498.1:n.1663+89T=
XM_011536197.1:c.1570+89T=	XP_011534499.1:n.1570+89T=
XM_011536198.1:c.1474+89T=	XP_011534500.1:n.1474+89T=
XM_006715586.3:c.1474+89T=	XP_006715649.1:n.1474+89T=
XM_011536196.3:c.1663+89T=	XP_011534498.1:n.1663+89T=
XM_011536198.3:c.1474+89T=	XP_011534500.1:n.1474+89T=
XM_024446573.1:c.1684+89T=	XP_024302341.1:n.1684+89T=
XR_001743697.2:n.1715+89T=
XR_942606.2:n.1766+89T=
NM_032861.4:c.1684+89T= MANE Select	NP_116250.3:n.1684+89T=
NR_073096.2:n.1688T=