Canonical Allele Identifier: CA366266819

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158571571G>C (hg19) ; chr6:g.158150539G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158150539G>C , CM000668.2:g.158150539G>C	GRCh38
NC_000006.11:g.158571571G>C , CM000668.1:g.158571571G>C	GRCh37
NC_000006.10:g.158491559G>C	NCBI36
NG_032889.1:g.22742C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*13C>G	ENSP00000475855.1:n.*13C>G
ENST00000642244.1:c.179C>G	ENSP00000493554.1:p.Thr60Arg
ENST00000642903.1:c.179C>G	ENSP00000493559.1:p.Thr60Arg
ENST00000643093.1:n.229C>G
ENST00000644972.1:c.179C>G	ENSP00000496451.1:p.Thr60Arg
ENST00000645077.1:c.*13C>G	ENSP00000496113.1:n.*13C>G
ENST00000645172.1:c.*13C>G	ENSP00000495367.1:n.*13C>G
ENST00000646190.1:n.1410C>G
ENST00000646208.1:c.92-3626C>G	ENSP00000493723.1:n.92-3626C>G
ENST00000646410.1:c.140C>G	ENSP00000494205.1:p.Thr47Arg
ENST00000646562.1:c.*13C>G	ENSP00000496087.1:n.*13C>G
ENST00000647468.2:c.179C>G MANE Select	ENSP00000496731.1:p.Thr60Arg
ENST00000648111.1:c.153C>G	ENSP00000497275.1:p.Asp51Glu
ENST00000367101.5:c.179C>G	ENSP00000356068.1:p.Thr60Arg
ENST00000367104.7:c.179C>G	ENSP00000356071.3:p.Thr60Arg
ENST00000606965.5:c.179C>G	ENSP00000475808.1:p.Thr60Arg
ENST00000607000.1:c.179C>G	ENSP00000475788.1:p.Thr60Arg
ENST00000607071.5:c.*13C>G	ENSP00000475855.1:n.*13C>G
ENST00000607742.5:c.*13C>G	ENSP00000475523.1:n.*13C>G
NM_032861.3:c.179C>G	NP_116250.3:p.Thr60Arg
NR_073096.1:n.321C>G
XM_006715586.1:c.-32C>G	XP_006715649.1:n.-32C>G
XM_011536196.1:c.158C>G	XP_011534498.1:p.Thr53Arg
XM_011536197.1:c.179C>G	XP_011534499.1:p.Thr60Arg
XM_011536198.1:c.-32C>G	XP_011534500.1:n.-32C>G
XR_942606.1:n.180C>G
XM_006715586.3:c.-32C>G	XP_006715649.1:n.-32C>G
XM_011536196.3:c.158C>G	XP_011534498.1:p.Thr53Arg
XM_011536198.3:c.-32C>G	XP_011534500.1:n.-32C>G
XM_024446573.1:c.179C>G	XP_024302341.1:p.Thr60Arg
XR_001743697.2:n.260C>G
XR_942606.2:n.311C>G
NM_032861.4:c.179C>G MANE Select	NP_116250.3:p.Thr60Arg
NR_073096.2:n.303C>G