Canonical Allele Identifier: CA366255137

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114907-G-T
• MyVariant Identifiers: chr6:g.158535939G>T (hg19) ; chr6:g.158114907G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114907G>T , CM000668.2:g.158114907G>T	GRCh38
NC_000006.11:g.158535939G>T , CM000668.1:g.158535939G>T	GRCh37
NC_000006.10:g.158455927G>T	NCBI36
NG_032889.1:g.58374C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.778C>A	ENSP00000391168.2:n.778C>A
ENST00000607071.6:c.*1286C>A	ENSP00000475855.1:n.*1286C>A
ENST00000642244.1:c.1476C>A	ENSP00000493554.1:p.Asn492Lys
ENST00000642903.1:c.1566C>A	ENSP00000493559.1:p.Asn522Lys
ENST00000644972.1:c.1566C>A	ENSP00000496451.1:p.Asn522Lys
ENST00000645077.1:c.*1187C>A	ENSP00000496113.1:n.*1187C>A
ENST00000645172.1:c.*1268C>A	ENSP00000495367.1:n.*1268C>A
ENST00000646190.1:n.2897C>A
ENST00000646208.1:c.1302C>A	ENSP00000493723.1:p.Asn434Lys
ENST00000646410.1:c.1437C>A	ENSP00000494205.1:p.Asn479Lys
ENST00000646562.1:c.*1400C>A	ENSP00000496087.1:n.*1400C>A
ENST00000647468.2:c.1566C>A MANE Select	ENSP00000496731.1:p.Asn522Lys
ENST00000648111.1:c.*1254C>A	ENSP00000497275.1:n.*1254C>A
ENST00000367101.5:c.*14C>A	ENSP00000356068.1:n.*14C>A
ENST00000367104.7:c.1566C>A	ENSP00000356071.3:p.Asn522Lys
ENST00000435180.5:c.291C>A	ENSP00000391168.1:p.Asn97Lys
ENST00000606965.5:c.*127C>A	ENSP00000475808.1:n.*127C>A
ENST00000607071.5:c.*1500C>A	ENSP00000475855.1:n.*1500C>A
ENST00000607742.5:c.*2844C>A	ENSP00000475523.1:n.*2844C>A
NM_032861.3:c.1566C>A	NP_116250.3:p.Asn522Lys
NR_073096.1:n.1499C>A
XM_006715586.1:c.1356C>A	XP_006715649.1:p.Asn452Lys
XM_011536196.1:c.1545C>A	XP_011534498.1:p.Asn515Lys
XM_011536197.1:c.1452C>A	XP_011534499.1:p.Asn484Lys
XM_011536198.1:c.1356C>A	XP_011534500.1:p.Asn452Lys
XM_006715586.3:c.1356C>A	XP_006715649.1:p.Asn452Lys
XM_011536196.3:c.1545C>A	XP_011534498.1:p.Asn515Lys
XM_011536198.3:c.1356C>A	XP_011534500.1:p.Asn452Lys
XM_024446573.1:c.1566C>A	XP_024302341.1:p.Asn522Lys
XR_001743697.2:n.1597C>A
XR_942606.2:n.1648C>A
NM_032861.4:c.1566C>A MANE Select	NP_116250.3:p.Asn522Lys
NR_073096.2:n.1481C>A