Canonical Allele Identifier: CA452820101

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535873A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114841A>G , CM000668.2:g.158114841A>G	GRCh38
NC_000006.11:g.158535873A>G , CM000668.1:g.158535873A>G	GRCh37
NC_000006.10:g.158455861A>G	NCBI36
NG_032889.1:g.58440T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.844T>C	ENSP00000391168.2:n.844T>C
ENST00000607071.6:c.*1352T>C	ENSP00000475855.1:n.*1352T>C
ENST00000642244.1:c.1542T>C	ENSP00000493554.1:p.Val514=
ENST00000642903.1:c.1632T>C	ENSP00000493559.1:p.Val544=
ENST00000644972.1:c.1632T>C	ENSP00000496451.1:p.Val544=
ENST00000645077.1:c.*1253T>C	ENSP00000496113.1:n.*1253T>C
ENST00000645172.1:c.*1334T>C	ENSP00000495367.1:n.*1334T>C
ENST00000646190.1:n.2963T>C
ENST00000646208.1:c.1368T>C	ENSP00000493723.1:p.Val456=
ENST00000646410.1:c.1503T>C	ENSP00000494205.1:p.Val501=
ENST00000646562.1:c.*1466T>C	ENSP00000496087.1:n.*1466T>C
ENST00000647468.2:c.1632T>C MANE Select	ENSP00000496731.1:p.Val544=
ENST00000648111.1:c.*1320T>C	ENSP00000497275.1:n.*1320T>C
ENST00000367101.5:c.*80T>C	ENSP00000356068.1:n.*80T>C
ENST00000367104.7:c.1632T>C	ENSP00000356071.3:p.Val544=
ENST00000435180.5:c.357T>C	ENSP00000391168.1:p.Val119=
ENST00000606965.5:c.*193T>C	ENSP00000475808.1:n.*193T>C
ENST00000607071.5:c.*1566T>C	ENSP00000475855.1:n.*1566T>C
ENST00000607742.5:c.*2910T>C	ENSP00000475523.1:n.*2910T>C
NM_032861.3:c.1632T>C	NP_116250.3:p.Val544=
NR_073096.1:n.1565T>C
XM_006715586.1:c.1422T>C	XP_006715649.1:p.Val474=
XM_011536196.1:c.1611T>C	XP_011534498.1:p.Val537=
XM_011536197.1:c.1518T>C	XP_011534499.1:p.Val506=
XM_011536198.1:c.1422T>C	XP_011534500.1:p.Val474=
XM_006715586.3:c.1422T>C	XP_006715649.1:p.Val474=
XM_011536196.3:c.1611T>C	XP_011534498.1:p.Val537=
XM_011536198.3:c.1422T>C	XP_011534500.1:p.Val474=
XM_024446573.1:c.1632T>C	XP_024302341.1:p.Val544=
XR_001743697.2:n.1663T>C
XR_942606.2:n.1714T>C
NM_032861.4:c.1632T>C MANE Select	NP_116250.3:p.Val544=
NR_073096.2:n.1547T>C