Canonical Allele Identifier: CA4071022

Gene: SERAC1

Linked Data

• dbSNP Id: rs376858726
• ExAC: 6:158535940 T / C
• gnomAD v2: 6-158535940-T-C
• gnomAD v3: 6-158114908-T-C
• gnomAD v4: 6-158114908-T-C
• MyVariant Identifiers: chr6:g.158535940T>C (hg19) ; chr6:g.158114908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114908T>C , CM000668.2:g.158114908T>C	GRCh38
NC_000006.11:g.158535940T>C , CM000668.1:g.158535940T>C	GRCh37
NC_000006.10:g.158455928T>C	NCBI36
NG_032889.1:g.58373A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.777A>G	ENSP00000391168.2:n.777A>G
ENST00000607071.6:c.*1285A>G	ENSP00000475855.1:n.*1285A>G
ENST00000642244.1:c.1475A>G	ENSP00000493554.1:p.Asn492Ser
ENST00000642903.1:c.1565A>G	ENSP00000493559.1:p.Asn522Ser
ENST00000644972.1:c.1565A>G	ENSP00000496451.1:p.Asn522Ser
ENST00000645077.1:c.*1186A>G	ENSP00000496113.1:n.*1186A>G
ENST00000645172.1:c.*1267A>G	ENSP00000495367.1:n.*1267A>G
ENST00000646190.1:n.2896A>G
ENST00000646208.1:c.1301A>G	ENSP00000493723.1:p.Asn434Ser
ENST00000646410.1:c.1436A>G	ENSP00000494205.1:p.Asn479Ser
ENST00000646562.1:c.*1399A>G	ENSP00000496087.1:n.*1399A>G
ENST00000647468.2:c.1565A>G MANE Select	ENSP00000496731.1:p.Asn522Ser
ENST00000648111.1:c.*1253A>G	ENSP00000497275.1:n.*1253A>G
ENST00000367101.5:c.*13A>G	ENSP00000356068.1:n.*13A>G
ENST00000367104.7:c.1565A>G	ENSP00000356071.3:p.Asn522Ser
ENST00000435180.5:c.290A>G	ENSP00000391168.1:p.Asn97Ser
ENST00000606965.5:c.*126A>G	ENSP00000475808.1:n.*126A>G
ENST00000607071.5:c.*1499A>G	ENSP00000475855.1:n.*1499A>G
ENST00000607742.5:c.*2843A>G	ENSP00000475523.1:n.*2843A>G
NM_032861.3:c.1565A>G	NP_116250.3:p.Asn522Ser
NR_073096.1:n.1498A>G
XM_006715586.1:c.1355A>G	XP_006715649.1:p.Asn452Ser
XM_011536196.1:c.1544A>G	XP_011534498.1:p.Asn515Ser
XM_011536197.1:c.1451A>G	XP_011534499.1:p.Asn484Ser
XM_011536198.1:c.1355A>G	XP_011534500.1:p.Asn452Ser
XM_006715586.3:c.1355A>G	XP_006715649.1:p.Asn452Ser
XM_011536196.3:c.1544A>G	XP_011534498.1:p.Asn515Ser
XM_011536198.3:c.1355A>G	XP_011534500.1:p.Asn452Ser
XM_024446573.1:c.1565A>G	XP_024302341.1:p.Asn522Ser
XR_001743697.2:n.1596A>G
XR_942606.2:n.1647A>G
NM_032861.4:c.1565A>G MANE Select	NP_116250.3:p.Asn522Ser
NR_073096.2:n.1480A>G