Canonical Allele Identifier: CA366264876

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567918T>G (hg19) ; chr6:g.158146886T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146886T>G , CM000668.2:g.158146886T>G	GRCh38
NC_000006.11:g.158567918T>G , CM000668.1:g.158567918T>G	GRCh37
NC_000006.10:g.158487906T>G	NCBI36
NG_032889.1:g.26395A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*217A>C	ENSP00000475855.1:n.*217A>C
ENST00000642244.1:c.293A>C	ENSP00000493554.1:p.Asp98Ala
ENST00000642903.1:c.383A>C	ENSP00000493559.1:p.Asp128Ala
ENST00000643093.1:n.433A>C
ENST00000644972.1:c.383A>C	ENSP00000496451.1:p.Asp128Ala
ENST00000645077.1:c.*217A>C	ENSP00000496113.1:n.*217A>C
ENST00000645172.1:c.*189+1979A>C	ENSP00000495367.1:n.*189+1979A>C
ENST00000646190.1:n.1614A>C
ENST00000646208.1:c.119A>C	ENSP00000493723.1:p.Asp40Ala
ENST00000646410.1:c.254A>C	ENSP00000494205.1:p.Asp85Ala
ENST00000646562.1:c.*217A>C	ENSP00000496087.1:n.*217A>C
ENST00000647468.2:c.383A>C MANE Select	ENSP00000496731.1:p.Asp128Ala
ENST00000648111.1:c.*27A>C	ENSP00000497275.1:n.*27A>C
ENST00000367101.5:c.383A>C	ENSP00000356068.1:p.Asp128Ala
ENST00000367104.7:c.383A>C	ENSP00000356071.3:p.Asp128Ala
ENST00000606965.5:c.383A>C	ENSP00000475808.1:p.Asp128Ala
ENST00000607000.1:c.383A>C	ENSP00000475788.1:p.Asp128Ala
ENST00000607071.5:c.*217A>C	ENSP00000475855.1:n.*217A>C
ENST00000607742.5:c.*217A>C	ENSP00000475523.1:n.*217A>C
NM_032861.3:c.383A>C	NP_116250.3:p.Asp128Ala
NR_073096.1:n.525A>C
XM_006715586.1:c.173A>C	XP_006715649.1:p.Asp58Ala
XM_011536196.1:c.362A>C	XP_011534498.1:p.Asp121Ala
XM_011536197.1:c.383A>C	XP_011534499.1:p.Asp128Ala
XM_011536198.1:c.173A>C	XP_011534500.1:p.Asp58Ala
XR_942606.1:n.384A>C
XM_006715586.3:c.173A>C	XP_006715649.1:p.Asp58Ala
XM_011536196.3:c.362A>C	XP_011534498.1:p.Asp121Ala
XM_011536198.3:c.173A>C	XP_011534500.1:p.Asp58Ala
XM_024446573.1:c.383A>C	XP_024302341.1:p.Asp128Ala
XR_001743697.2:n.464A>C
XR_942606.2:n.515A>C
NM_032861.4:c.383A>C MANE Select	NP_116250.3:p.Asp128Ala
NR_073096.2:n.507A>C