Canonical Allele Identifier: CA366264865

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567916G>C (hg19) ; chr6:g.158146884G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146884G>C , CM000668.2:g.158146884G>C	GRCh38
NC_000006.11:g.158567916G>C , CM000668.1:g.158567916G>C	GRCh37
NC_000006.10:g.158487904G>C	NCBI36
NG_032889.1:g.26397C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*219C>G	ENSP00000475855.1:n.*219C>G
ENST00000642244.1:c.295C>G	ENSP00000493554.1:p.His99Asp
ENST00000642903.1:c.385C>G	ENSP00000493559.1:p.His129Asp
ENST00000643093.1:n.435C>G
ENST00000644972.1:c.385C>G	ENSP00000496451.1:p.His129Asp
ENST00000645077.1:c.*219C>G	ENSP00000496113.1:n.*219C>G
ENST00000645172.1:c.*189+1981C>G	ENSP00000495367.1:n.*189+1981C>G
ENST00000646190.1:n.1616C>G
ENST00000646208.1:c.121C>G	ENSP00000493723.1:p.His41Asp
ENST00000646410.1:c.256C>G	ENSP00000494205.1:p.His86Asp
ENST00000646562.1:c.*219C>G	ENSP00000496087.1:n.*219C>G
ENST00000647468.2:c.385C>G MANE Select	ENSP00000496731.1:p.His129Asp
ENST00000648111.1:c.*29C>G	ENSP00000497275.1:n.*29C>G
ENST00000367101.5:c.385C>G	ENSP00000356068.1:p.His129Asp
ENST00000367104.7:c.385C>G	ENSP00000356071.3:p.His129Asp
ENST00000606965.5:c.385C>G	ENSP00000475808.1:p.His129Asp
ENST00000607000.1:c.385C>G	ENSP00000475788.1:p.His129Asp
ENST00000607071.5:c.*219C>G	ENSP00000475855.1:n.*219C>G
ENST00000607742.5:c.*219C>G	ENSP00000475523.1:n.*219C>G
NM_032861.3:c.385C>G	NP_116250.3:p.His129Asp
NR_073096.1:n.527C>G
XM_006715586.1:c.175C>G	XP_006715649.1:p.His59Asp
XM_011536196.1:c.364C>G	XP_011534498.1:p.His122Asp
XM_011536197.1:c.385C>G	XP_011534499.1:p.His129Asp
XM_011536198.1:c.175C>G	XP_011534500.1:p.His59Asp
XR_942606.1:n.386C>G
XM_006715586.3:c.175C>G	XP_006715649.1:p.His59Asp
XM_011536196.3:c.364C>G	XP_011534498.1:p.His122Asp
XM_011536198.3:c.175C>G	XP_011534500.1:p.His59Asp
XM_024446573.1:c.385C>G	XP_024302341.1:p.His129Asp
XR_001743697.2:n.466C>G
XR_942606.2:n.517C>G
NM_032861.4:c.385C>G MANE Select	NP_116250.3:p.His129Asp
NR_073096.2:n.509C>G