Canonical Allele Identifier: CA366264892

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567920T>G (hg19) ; chr6:g.158146888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146888T>G , CM000668.2:g.158146888T>G	GRCh38
NC_000006.11:g.158567920T>G , CM000668.1:g.158567920T>G	GRCh37
NC_000006.10:g.158487908T>G	NCBI36
NG_032889.1:g.26393A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*215A>C	ENSP00000475855.1:n.*215A>C
ENST00000642244.1:c.291A>C	ENSP00000493554.1:p.Glu97Asp
ENST00000642903.1:c.381A>C	ENSP00000493559.1:p.Glu127Asp
ENST00000643093.1:n.431A>C
ENST00000644972.1:c.381A>C	ENSP00000496451.1:p.Glu127Asp
ENST00000645077.1:c.*215A>C	ENSP00000496113.1:n.*215A>C
ENST00000645172.1:c.*189+1977A>C	ENSP00000495367.1:n.*189+1977A>C
ENST00000646190.1:n.1612A>C
ENST00000646208.1:c.117A>C	ENSP00000493723.1:p.Glu39Asp
ENST00000646410.1:c.252A>C	ENSP00000494205.1:p.Glu84Asp
ENST00000646562.1:c.*215A>C	ENSP00000496087.1:n.*215A>C
ENST00000647468.2:c.381A>C MANE Select	ENSP00000496731.1:p.Glu127Asp
ENST00000648111.1:c.*25A>C	ENSP00000497275.1:n.*25A>C
ENST00000367101.5:c.381A>C	ENSP00000356068.1:p.Glu127Asp
ENST00000367104.7:c.381A>C	ENSP00000356071.3:p.Glu127Asp
ENST00000606965.5:c.381A>C	ENSP00000475808.1:p.Glu127Asp
ENST00000607000.1:c.381A>C	ENSP00000475788.1:p.Glu127Asp
ENST00000607071.5:c.*215A>C	ENSP00000475855.1:n.*215A>C
ENST00000607742.5:c.*215A>C	ENSP00000475523.1:n.*215A>C
NM_032861.3:c.381A>C	NP_116250.3:p.Glu127Asp
NR_073096.1:n.523A>C
XM_006715586.1:c.171A>C	XP_006715649.1:p.Glu57Asp
XM_011536196.1:c.360A>C	XP_011534498.1:p.Glu120Asp
XM_011536197.1:c.381A>C	XP_011534499.1:p.Glu127Asp
XM_011536198.1:c.171A>C	XP_011534500.1:p.Glu57Asp
XR_942606.1:n.382A>C
XM_006715586.3:c.171A>C	XP_006715649.1:p.Glu57Asp
XM_011536196.3:c.360A>C	XP_011534498.1:p.Glu120Asp
XM_011536198.3:c.171A>C	XP_011534500.1:p.Glu57Asp
XM_024446573.1:c.381A>C	XP_024302341.1:p.Glu127Asp
XR_001743697.2:n.462A>C
XR_942606.2:n.513A>C
NM_032861.4:c.381A>C MANE Select	NP_116250.3:p.Glu127Asp
NR_073096.2:n.505A>C