Canonical Allele Identifier: CA366255281

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535994A>C (hg19) ; chr6:g.158114962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114962A>C , CM000668.2:g.158114962A>C	GRCh38
NC_000006.11:g.158535994A>C , CM000668.1:g.158535994A>C	GRCh37
NC_000006.10:g.158455982A>C	NCBI36
NG_032889.1:g.58319T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.723T>G	ENSP00000391168.2:n.723T>G
ENST00000607071.6:c.*1231T>G	ENSP00000475855.1:n.*1231T>G
ENST00000642244.1:c.1421T>G	ENSP00000493554.1:p.Val474Gly
ENST00000642903.1:c.1511T>G	ENSP00000493559.1:p.Val504Gly
ENST00000644972.1:c.1511T>G	ENSP00000496451.1:p.Val504Gly
ENST00000645077.1:c.*1132T>G	ENSP00000496113.1:n.*1132T>G
ENST00000645172.1:c.*1213T>G	ENSP00000495367.1:n.*1213T>G
ENST00000646190.1:n.2842T>G
ENST00000646208.1:c.1247T>G	ENSP00000493723.1:p.Val416Gly
ENST00000646410.1:c.1382T>G	ENSP00000494205.1:p.Val461Gly
ENST00000646562.1:c.*1345T>G	ENSP00000496087.1:n.*1345T>G
ENST00000647468.2:c.1511T>G MANE Select	ENSP00000496731.1:p.Val504Gly
ENST00000648111.1:c.*1199T>G	ENSP00000497275.1:n.*1199T>G
ENST00000367101.5:c.1555T>G	ENSP00000356068.1:p.Ser519Ala
ENST00000367104.7:c.1511T>G	ENSP00000356071.3:p.Val504Gly
ENST00000435180.5:c.236T>G	ENSP00000391168.1:p.Val79Gly
ENST00000606965.5:c.*72T>G	ENSP00000475808.1:n.*72T>G
ENST00000607071.5:c.*1445T>G	ENSP00000475855.1:n.*1445T>G
ENST00000607742.5:c.*2789T>G	ENSP00000475523.1:n.*2789T>G
NM_032861.3:c.1511T>G	NP_116250.3:p.Val504Gly
NR_073096.1:n.1444T>G
XM_006715586.1:c.1301T>G	XP_006715649.1:p.Val434Gly
XM_011536196.1:c.1490T>G	XP_011534498.1:p.Val497Gly
XM_011536197.1:c.1397T>G	XP_011534499.1:p.Val466Gly
XM_011536198.1:c.1301T>G	XP_011534500.1:p.Val434Gly
XM_006715586.3:c.1301T>G	XP_006715649.1:p.Val434Gly
XM_011536196.3:c.1490T>G	XP_011534498.1:p.Val497Gly
XM_011536198.3:c.1301T>G	XP_011534500.1:p.Val434Gly
XM_024446573.1:c.1511T>G	XP_024302341.1:p.Val504Gly
XR_001743697.2:n.1542T>G
XR_942606.2:n.1593T>G
NM_032861.4:c.1511T>G MANE Select	NP_116250.3:p.Val504Gly
NR_073096.2:n.1426T>G