Canonical Allele Identifier: CA366264559

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567824A>C (hg19) ; chr6:g.158146792A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146792A>C , CM000668.2:g.158146792A>C	GRCh38
NC_000006.11:g.158567824A>C , CM000668.1:g.158567824A>C	GRCh37
NC_000006.10:g.158487812A>C	NCBI36
NG_032889.1:g.26489T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*311T>G	ENSP00000475855.1:n.*311T>G
ENST00000642244.1:c.387T>G	ENSP00000493554.1:p.His129Gln
ENST00000642903.1:c.477T>G	ENSP00000493559.1:p.His159Gln
ENST00000644972.1:c.477T>G	ENSP00000496451.1:p.His159Gln
ENST00000645077.1:c.*311T>G	ENSP00000496113.1:n.*311T>G
ENST00000645172.1:c.*189+2073T>G	ENSP00000495367.1:n.*189+2073T>G
ENST00000646190.1:n.1708T>G
ENST00000646208.1:c.213T>G	ENSP00000493723.1:p.His71Gln
ENST00000646410.1:c.348T>G	ENSP00000494205.1:p.His116Gln
ENST00000646562.1:c.*311T>G	ENSP00000496087.1:n.*311T>G
ENST00000647468.2:c.477T>G MANE Select	ENSP00000496731.1:p.His159Gln
ENST00000648111.1:c.*121T>G	ENSP00000497275.1:n.*121T>G
ENST00000367101.5:c.477T>G	ENSP00000356068.1:p.His159Gln
ENST00000367104.7:c.477T>G	ENSP00000356071.3:p.His159Gln
ENST00000606965.5:c.477T>G	ENSP00000475808.1:p.His159Gln
ENST00000607000.1:c.477T>G	ENSP00000475788.1:p.His159Gln
ENST00000607071.5:c.*311T>G	ENSP00000475855.1:n.*311T>G
ENST00000607742.5:c.*311T>G	ENSP00000475523.1:n.*311T>G
NM_032861.3:c.477T>G	NP_116250.3:p.His159Gln
NR_073096.1:n.619T>G
XM_006715586.1:c.267T>G	XP_006715649.1:p.His89Gln
XM_011536196.1:c.456T>G	XP_011534498.1:p.His152Gln
XM_011536197.1:c.477T>G	XP_011534499.1:p.His159Gln
XM_011536198.1:c.267T>G	XP_011534500.1:p.His89Gln
XR_942606.1:n.478T>G
XM_006715586.3:c.267T>G	XP_006715649.1:p.His89Gln
XM_011536196.3:c.456T>G	XP_011534498.1:p.His152Gln
XM_011536198.3:c.267T>G	XP_011534500.1:p.His89Gln
XM_024446573.1:c.477T>G	XP_024302341.1:p.His159Gln
XR_001743697.2:n.558T>G
XR_942606.2:n.609T>G
NM_032861.4:c.477T>G MANE Select	NP_116250.3:p.His159Gln
NR_073096.2:n.601T>G