Canonical Allele Identifier: CA366264537

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567816T>A (hg19) ; chr6:g.158146784T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146784T>A , CM000668.2:g.158146784T>A	GRCh38
NC_000006.11:g.158567816T>A , CM000668.1:g.158567816T>A	GRCh37
NC_000006.10:g.158487804T>A	NCBI36
NG_032889.1:g.26497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*319A>T	ENSP00000475855.1:n.*319A>T
ENST00000642244.1:c.395A>T	ENSP00000493554.1:p.His132Leu
ENST00000642903.1:c.485A>T	ENSP00000493559.1:p.His162Leu
ENST00000644972.1:c.485A>T	ENSP00000496451.1:p.His162Leu
ENST00000645077.1:c.*319A>T	ENSP00000496113.1:n.*319A>T
ENST00000645172.1:c.*189+2081A>T	ENSP00000495367.1:n.*189+2081A>T
ENST00000646190.1:n.1716A>T
ENST00000646208.1:c.221A>T	ENSP00000493723.1:p.His74Leu
ENST00000646410.1:c.356A>T	ENSP00000494205.1:p.His119Leu
ENST00000646562.1:c.*319A>T	ENSP00000496087.1:n.*319A>T
ENST00000647468.2:c.485A>T MANE Select	ENSP00000496731.1:p.His162Leu
ENST00000648111.1:c.*129A>T	ENSP00000497275.1:n.*129A>T
ENST00000367101.5:c.485A>T	ENSP00000356068.1:p.His162Leu
ENST00000367104.7:c.485A>T	ENSP00000356071.3:p.His162Leu
ENST00000606965.5:c.485A>T	ENSP00000475808.1:p.His162Leu
ENST00000607000.1:c.485A>T	ENSP00000475788.1:p.His162Leu
ENST00000607071.5:c.*319A>T	ENSP00000475855.1:n.*319A>T
ENST00000607742.5:c.*319A>T	ENSP00000475523.1:n.*319A>T
NM_032861.3:c.485A>T	NP_116250.3:p.His162Leu
NR_073096.1:n.627A>T
XM_006715586.1:c.275A>T	XP_006715649.1:p.His92Leu
XM_011536196.1:c.464A>T	XP_011534498.1:p.His155Leu
XM_011536197.1:c.485A>T	XP_011534499.1:p.His162Leu
XM_011536198.1:c.275A>T	XP_011534500.1:p.His92Leu
XR_942606.1:n.486A>T
XM_006715586.3:c.275A>T	XP_006715649.1:p.His92Leu
XM_011536196.3:c.464A>T	XP_011534498.1:p.His155Leu
XM_011536198.3:c.275A>T	XP_011534500.1:p.His92Leu
XM_024446573.1:c.485A>T	XP_024302341.1:p.His162Leu
XR_001743697.2:n.566A>T
XR_942606.2:n.617A>T
NM_032861.4:c.485A>T MANE Select	NP_116250.3:p.His162Leu
NR_073096.2:n.609A>T