Canonical Allele Identifier: CA366254968

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535862T>A (hg19) ; chr6:g.158114830T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114830T>A , CM000668.2:g.158114830T>A	GRCh38
NC_000006.11:g.158535862T>A , CM000668.1:g.158535862T>A	GRCh37
NC_000006.10:g.158455850T>A	NCBI36
NG_032889.1:g.58451A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.855A>T	ENSP00000391168.2:n.855A>T
ENST00000607071.6:c.*1363A>T	ENSP00000475855.1:n.*1363A>T
ENST00000642244.1:c.1553A>T	ENSP00000493554.1:p.Tyr518Phe
ENST00000642903.1:c.1643A>T	ENSP00000493559.1:p.Tyr548Phe
ENST00000644972.1:c.1643A>T	ENSP00000496451.1:p.Tyr548Phe
ENST00000645077.1:c.*1264A>T	ENSP00000496113.1:n.*1264A>T
ENST00000645172.1:c.*1345A>T	ENSP00000495367.1:n.*1345A>T
ENST00000646190.1:n.2974A>T
ENST00000646208.1:c.1379A>T	ENSP00000493723.1:p.Tyr460Phe
ENST00000646410.1:c.1514A>T	ENSP00000494205.1:p.Tyr505Phe
ENST00000646562.1:c.*1477A>T	ENSP00000496087.1:n.*1477A>T
ENST00000647468.2:c.1643A>T MANE Select	ENSP00000496731.1:p.Tyr548Phe
ENST00000648111.1:c.*1331A>T	ENSP00000497275.1:n.*1331A>T
ENST00000367101.5:c.*91A>T	ENSP00000356068.1:n.*91A>T
ENST00000367104.7:c.1643A>T	ENSP00000356071.3:p.Tyr548Phe
ENST00000435180.5:c.368A>T	ENSP00000391168.1:p.Tyr123Phe
ENST00000606965.5:c.*204A>T	ENSP00000475808.1:n.*204A>T
ENST00000607071.5:c.*1577A>T	ENSP00000475855.1:n.*1577A>T
ENST00000607742.5:c.*2921A>T	ENSP00000475523.1:n.*2921A>T
NM_032861.3:c.1643A>T	NP_116250.3:p.Tyr548Phe
NR_073096.1:n.1576A>T
XM_006715586.1:c.1433A>T	XP_006715649.1:p.Tyr478Phe
XM_011536196.1:c.1622A>T	XP_011534498.1:p.Tyr541Phe
XM_011536197.1:c.1529A>T	XP_011534499.1:p.Tyr510Phe
XM_011536198.1:c.1433A>T	XP_011534500.1:p.Tyr478Phe
XM_006715586.3:c.1433A>T	XP_006715649.1:p.Tyr478Phe
XM_011536196.3:c.1622A>T	XP_011534498.1:p.Tyr541Phe
XM_011536198.3:c.1433A>T	XP_011534500.1:p.Tyr478Phe
XM_024446573.1:c.1643A>T	XP_024302341.1:p.Tyr548Phe
XR_001743697.2:n.1674A>T
XR_942606.2:n.1725A>T
NM_032861.4:c.1643A>T MANE Select	NP_116250.3:p.Tyr548Phe
NR_073096.2:n.1558A>T