Canonical Allele Identifier: CA366255165

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535952C>T (hg19) ; chr6:g.158114920C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114920C>T , CM000668.2:g.158114920C>T	GRCh38
NC_000006.11:g.158535952C>T , CM000668.1:g.158535952C>T	GRCh37
NC_000006.10:g.158455940C>T	NCBI36
NG_032889.1:g.58361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.765G>A	ENSP00000391168.2:n.765G>A
ENST00000607071.6:c.*1273G>A	ENSP00000475855.1:n.*1273G>A
ENST00000642244.1:c.1463G>A	ENSP00000493554.1:p.Ser488Asn
ENST00000642903.1:c.1553G>A	ENSP00000493559.1:p.Ser518Asn
ENST00000644972.1:c.1553G>A	ENSP00000496451.1:p.Ser518Asn
ENST00000645077.1:c.*1174G>A	ENSP00000496113.1:n.*1174G>A
ENST00000645172.1:c.*1255G>A	ENSP00000495367.1:n.*1255G>A
ENST00000646190.1:n.2884G>A
ENST00000646208.1:c.1289G>A	ENSP00000493723.1:p.Ser430Asn
ENST00000646410.1:c.1424G>A	ENSP00000494205.1:p.Ser475Asn
ENST00000646562.1:c.*1387G>A	ENSP00000496087.1:n.*1387G>A
ENST00000647468.2:c.1553G>A MANE Select	ENSP00000496731.1:p.Ser518Asn
ENST00000648111.1:c.*1241G>A	ENSP00000497275.1:n.*1241G>A
ENST00000367101.5:c.*1G>A	ENSP00000356068.1:n.*1G>A
ENST00000367104.7:c.1553G>A	ENSP00000356071.3:p.Ser518Asn
ENST00000435180.5:c.278G>A	ENSP00000391168.1:p.Ser93Asn
ENST00000606965.5:c.*114G>A	ENSP00000475808.1:n.*114G>A
ENST00000607071.5:c.*1487G>A	ENSP00000475855.1:n.*1487G>A
ENST00000607742.5:c.*2831G>A	ENSP00000475523.1:n.*2831G>A
NM_032861.3:c.1553G>A	NP_116250.3:p.Ser518Asn
NR_073096.1:n.1486G>A
XM_006715586.1:c.1343G>A	XP_006715649.1:p.Ser448Asn
XM_011536196.1:c.1532G>A	XP_011534498.1:p.Ser511Asn
XM_011536197.1:c.1439G>A	XP_011534499.1:p.Ser480Asn
XM_011536198.1:c.1343G>A	XP_011534500.1:p.Ser448Asn
XM_006715586.3:c.1343G>A	XP_006715649.1:p.Ser448Asn
XM_011536196.3:c.1532G>A	XP_011534498.1:p.Ser511Asn
XM_011536198.3:c.1343G>A	XP_011534500.1:p.Ser448Asn
XM_024446573.1:c.1553G>A	XP_024302341.1:p.Ser518Asn
XR_001743697.2:n.1584G>A
XR_942606.2:n.1635G>A
NM_032861.4:c.1553G>A MANE Select	NP_116250.3:p.Ser518Asn
NR_073096.2:n.1468G>A