Canonical Allele Identifier: CA366255023

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535887C>T (hg19) ; chr6:g.158114855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114855C>T , CM000668.2:g.158114855C>T	GRCh38
NC_000006.11:g.158535887C>T , CM000668.1:g.158535887C>T	GRCh37
NC_000006.10:g.158455875C>T	NCBI36
NG_032889.1:g.58426G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.830G>A	ENSP00000391168.2:n.830G>A
ENST00000607071.6:c.*1338G>A	ENSP00000475855.1:n.*1338G>A
ENST00000642244.1:c.1528G>A	ENSP00000493554.1:p.Ala510Thr
ENST00000642903.1:c.1618G>A	ENSP00000493559.1:p.Ala540Thr
ENST00000644972.1:c.1618G>A	ENSP00000496451.1:p.Ala540Thr
ENST00000645077.1:c.*1239G>A	ENSP00000496113.1:n.*1239G>A
ENST00000645172.1:c.*1320G>A	ENSP00000495367.1:n.*1320G>A
ENST00000646190.1:n.2949G>A
ENST00000646208.1:c.1354G>A	ENSP00000493723.1:p.Ala452Thr
ENST00000646410.1:c.1489G>A	ENSP00000494205.1:p.Ala497Thr
ENST00000646562.1:c.*1452G>A	ENSP00000496087.1:n.*1452G>A
ENST00000647468.2:c.1618G>A MANE Select	ENSP00000496731.1:p.Ala540Thr
ENST00000648111.1:c.*1306G>A	ENSP00000497275.1:n.*1306G>A
ENST00000367101.5:c.*66G>A	ENSP00000356068.1:n.*66G>A
ENST00000367104.7:c.1618G>A	ENSP00000356071.3:p.Ala540Thr
ENST00000435180.5:c.343G>A	ENSP00000391168.1:p.Ala115Thr
ENST00000606965.5:c.*179G>A	ENSP00000475808.1:n.*179G>A
ENST00000607071.5:c.*1552G>A	ENSP00000475855.1:n.*1552G>A
ENST00000607742.5:c.*2896G>A	ENSP00000475523.1:n.*2896G>A
NM_032861.3:c.1618G>A	NP_116250.3:p.Ala540Thr
NR_073096.1:n.1551G>A
XM_006715586.1:c.1408G>A	XP_006715649.1:p.Ala470Thr
XM_011536196.1:c.1597G>A	XP_011534498.1:p.Ala533Thr
XM_011536197.1:c.1504G>A	XP_011534499.1:p.Ala502Thr
XM_011536198.1:c.1408G>A	XP_011534500.1:p.Ala470Thr
XM_006715586.3:c.1408G>A	XP_006715649.1:p.Ala470Thr
XM_011536196.3:c.1597G>A	XP_011534498.1:p.Ala533Thr
XM_011536198.3:c.1408G>A	XP_011534500.1:p.Ala470Thr
XM_024446573.1:c.1618G>A	XP_024302341.1:p.Ala540Thr
XR_001743697.2:n.1649G>A
XR_942606.2:n.1700G>A
NM_032861.4:c.1618G>A MANE Select	NP_116250.3:p.Ala540Thr
NR_073096.2:n.1533G>A