Canonical Allele Identifier: CA366255063

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535907G>T (hg19) ; chr6:g.158114875G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114875G>T , CM000668.2:g.158114875G>T	GRCh38
NC_000006.11:g.158535907G>T , CM000668.1:g.158535907G>T	GRCh37
NC_000006.10:g.158455895G>T	NCBI36
NG_032889.1:g.58406C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.810C>A	ENSP00000391168.2:n.810C>A
ENST00000607071.6:c.*1318C>A	ENSP00000475855.1:n.*1318C>A
ENST00000642244.1:c.1508C>A	ENSP00000493554.1:p.Pro503His
ENST00000642903.1:c.1598C>A	ENSP00000493559.1:p.Pro533His
ENST00000644972.1:c.1598C>A	ENSP00000496451.1:p.Pro533His
ENST00000645077.1:c.*1219C>A	ENSP00000496113.1:n.*1219C>A
ENST00000645172.1:c.*1300C>A	ENSP00000495367.1:n.*1300C>A
ENST00000646190.1:n.2929C>A
ENST00000646208.1:c.1334C>A	ENSP00000493723.1:p.Pro445His
ENST00000646410.1:c.1469C>A	ENSP00000494205.1:p.Pro490His
ENST00000646562.1:c.*1432C>A	ENSP00000496087.1:n.*1432C>A
ENST00000647468.2:c.1598C>A MANE Select	ENSP00000496731.1:p.Pro533His
ENST00000648111.1:c.*1286C>A	ENSP00000497275.1:n.*1286C>A
ENST00000367101.5:c.*46C>A	ENSP00000356068.1:n.*46C>A
ENST00000367104.7:c.1598C>A	ENSP00000356071.3:p.Pro533His
ENST00000435180.5:c.323C>A	ENSP00000391168.1:p.Pro108His
ENST00000606965.5:c.*159C>A	ENSP00000475808.1:n.*159C>A
ENST00000607071.5:c.*1532C>A	ENSP00000475855.1:n.*1532C>A
ENST00000607742.5:c.*2876C>A	ENSP00000475523.1:n.*2876C>A
NM_032861.3:c.1598C>A	NP_116250.3:p.Pro533His
NR_073096.1:n.1531C>A
XM_006715586.1:c.1388C>A	XP_006715649.1:p.Pro463His
XM_011536196.1:c.1577C>A	XP_011534498.1:p.Pro526His
XM_011536197.1:c.1484C>A	XP_011534499.1:p.Pro495His
XM_011536198.1:c.1388C>A	XP_011534500.1:p.Pro463His
XM_006715586.3:c.1388C>A	XP_006715649.1:p.Pro463His
XM_011536196.3:c.1577C>A	XP_011534498.1:p.Pro526His
XM_011536198.3:c.1388C>A	XP_011534500.1:p.Pro463His
XM_024446573.1:c.1598C>A	XP_024302341.1:p.Pro533His
XR_001743697.2:n.1629C>A
XR_942606.2:n.1680C>A
NM_032861.4:c.1598C>A MANE Select	NP_116250.3:p.Pro533His
NR_073096.2:n.1513C>A