Canonical Allele Identifier: CA366255128

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535936A>C (hg19) ; chr6:g.158114904A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114904A>C , CM000668.2:g.158114904A>C	GRCh38
NC_000006.11:g.158535936A>C , CM000668.1:g.158535936A>C	GRCh37
NC_000006.10:g.158455924A>C	NCBI36
NG_032889.1:g.58377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.781T>G	ENSP00000391168.2:n.781T>G
ENST00000607071.6:c.*1289T>G	ENSP00000475855.1:n.*1289T>G
ENST00000642244.1:c.1479T>G	ENSP00000493554.1:p.Asn493Lys
ENST00000642903.1:c.1569T>G	ENSP00000493559.1:p.Asn523Lys
ENST00000644972.1:c.1569T>G	ENSP00000496451.1:p.Asn523Lys
ENST00000645077.1:c.*1190T>G	ENSP00000496113.1:n.*1190T>G
ENST00000645172.1:c.*1271T>G	ENSP00000495367.1:n.*1271T>G
ENST00000646190.1:n.2900T>G
ENST00000646208.1:c.1305T>G	ENSP00000493723.1:p.Asn435Lys
ENST00000646410.1:c.1440T>G	ENSP00000494205.1:p.Asn480Lys
ENST00000646562.1:c.*1403T>G	ENSP00000496087.1:n.*1403T>G
ENST00000647468.2:c.1569T>G MANE Select	ENSP00000496731.1:p.Asn523Lys
ENST00000648111.1:c.*1257T>G	ENSP00000497275.1:n.*1257T>G
ENST00000367101.5:c.*17T>G	ENSP00000356068.1:n.*17T>G
ENST00000367104.7:c.1569T>G	ENSP00000356071.3:p.Asn523Lys
ENST00000435180.5:c.294T>G	ENSP00000391168.1:p.Asn98Lys
ENST00000606965.5:c.*130T>G	ENSP00000475808.1:n.*130T>G
ENST00000607071.5:c.*1503T>G	ENSP00000475855.1:n.*1503T>G
ENST00000607742.5:c.*2847T>G	ENSP00000475523.1:n.*2847T>G
NM_032861.3:c.1569T>G	NP_116250.3:p.Asn523Lys
NR_073096.1:n.1502T>G
XM_006715586.1:c.1359T>G	XP_006715649.1:p.Asn453Lys
XM_011536196.1:c.1548T>G	XP_011534498.1:p.Asn516Lys
XM_011536197.1:c.1455T>G	XP_011534499.1:p.Asn485Lys
XM_011536198.1:c.1359T>G	XP_011534500.1:p.Asn453Lys
XM_006715586.3:c.1359T>G	XP_006715649.1:p.Asn453Lys
XM_011536196.3:c.1548T>G	XP_011534498.1:p.Asn516Lys
XM_011536198.3:c.1359T>G	XP_011534500.1:p.Asn453Lys
XM_024446573.1:c.1569T>G	XP_024302341.1:p.Asn523Lys
XR_001743697.2:n.1600T>G
XR_942606.2:n.1651T>G
NM_032861.4:c.1569T>G MANE Select	NP_116250.3:p.Asn523Lys
NR_073096.2:n.1484T>G