Canonical Allele Identifier: CA366264668

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567874C>G (hg19) ; chr6:g.158146842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146842C>G , CM000668.2:g.158146842C>G	GRCh38
NC_000006.11:g.158567874C>G , CM000668.1:g.158567874C>G	GRCh37
NC_000006.10:g.158487862C>G	NCBI36
NG_032889.1:g.26439G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*261G>C	ENSP00000475855.1:n.*261G>C
ENST00000642244.1:c.337G>C	ENSP00000493554.1:p.Asp113His
ENST00000642903.1:c.427G>C	ENSP00000493559.1:p.Asp143His
ENST00000644972.1:c.427G>C	ENSP00000496451.1:p.Asp143His
ENST00000645077.1:c.*261G>C	ENSP00000496113.1:n.*261G>C
ENST00000645172.1:c.*189+2023G>C	ENSP00000495367.1:n.*189+2023G>C
ENST00000646190.1:n.1658G>C
ENST00000646208.1:c.163G>C	ENSP00000493723.1:p.Asp55His
ENST00000646410.1:c.298G>C	ENSP00000494205.1:p.Asp100His
ENST00000646562.1:c.*261G>C	ENSP00000496087.1:n.*261G>C
ENST00000647468.2:c.427G>C MANE Select	ENSP00000496731.1:p.Asp143His
ENST00000648111.1:c.*71G>C	ENSP00000497275.1:n.*71G>C
ENST00000367101.5:c.427G>C	ENSP00000356068.1:p.Asp143His
ENST00000367104.7:c.427G>C	ENSP00000356071.3:p.Asp143His
ENST00000606965.5:c.427G>C	ENSP00000475808.1:p.Asp143His
ENST00000607000.1:c.427G>C	ENSP00000475788.1:p.Asp143His
ENST00000607071.5:c.*261G>C	ENSP00000475855.1:n.*261G>C
ENST00000607742.5:c.*261G>C	ENSP00000475523.1:n.*261G>C
NM_032861.3:c.427G>C	NP_116250.3:p.Asp143His
NR_073096.1:n.569G>C
XM_006715586.1:c.217G>C	XP_006715649.1:p.Asp73His
XM_011536196.1:c.406G>C	XP_011534498.1:p.Asp136His
XM_011536197.1:c.427G>C	XP_011534499.1:p.Asp143His
XM_011536198.1:c.217G>C	XP_011534500.1:p.Asp73His
XR_942606.1:n.428G>C
XM_006715586.3:c.217G>C	XP_006715649.1:p.Asp73His
XM_011536196.3:c.406G>C	XP_011534498.1:p.Asp136His
XM_011536198.3:c.217G>C	XP_011534500.1:p.Asp73His
XM_024446573.1:c.427G>C	XP_024302341.1:p.Asp143His
XR_001743697.2:n.508G>C
XR_942606.2:n.559G>C
NM_032861.4:c.427G>C MANE Select	NP_116250.3:p.Asp143His
NR_073096.2:n.551G>C