Canonical Allele Identifier: CA366264900

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567922C>A (hg19) ; chr6:g.158146890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146890C>A , CM000668.2:g.158146890C>A	GRCh38
NC_000006.11:g.158567922C>A , CM000668.1:g.158567922C>A	GRCh37
NC_000006.10:g.158487910C>A	NCBI36
NG_032889.1:g.26391G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*213G>T	ENSP00000475855.1:n.*213G>T
ENST00000642244.1:c.289G>T	ENSP00000493554.1:p.Glu97Ter
ENST00000642903.1:c.379G>T	ENSP00000493559.1:p.Glu127Ter
ENST00000643093.1:n.429G>T
ENST00000644972.1:c.379G>T	ENSP00000496451.1:p.Glu127Ter
ENST00000645077.1:c.*213G>T	ENSP00000496113.1:n.*213G>T
ENST00000645172.1:c.*189+1975G>T	ENSP00000495367.1:n.*189+1975G>T
ENST00000646190.1:n.1610G>T
ENST00000646208.1:c.115G>T	ENSP00000493723.1:p.Glu39Ter
ENST00000646410.1:c.250G>T	ENSP00000494205.1:p.Glu84Ter
ENST00000646562.1:c.*213G>T	ENSP00000496087.1:n.*213G>T
ENST00000647468.2:c.379G>T MANE Select	ENSP00000496731.1:p.Glu127Ter
ENST00000648111.1:c.*23G>T	ENSP00000497275.1:n.*23G>T
ENST00000367101.5:c.379G>T	ENSP00000356068.1:p.Glu127Ter
ENST00000367104.7:c.379G>T	ENSP00000356071.3:p.Glu127Ter
ENST00000606965.5:c.379G>T	ENSP00000475808.1:p.Glu127Ter
ENST00000607000.1:c.379G>T	ENSP00000475788.1:p.Glu127Ter
ENST00000607071.5:c.*213G>T	ENSP00000475855.1:n.*213G>T
ENST00000607742.5:c.*213G>T	ENSP00000475523.1:n.*213G>T
NM_032861.3:c.379G>T	NP_116250.3:p.Glu127Ter
NR_073096.1:n.521G>T
XM_006715586.1:c.169G>T	XP_006715649.1:p.Glu57Ter
XM_011536196.1:c.358G>T	XP_011534498.1:p.Glu120Ter
XM_011536197.1:c.379G>T	XP_011534499.1:p.Glu127Ter
XM_011536198.1:c.169G>T	XP_011534500.1:p.Glu57Ter
XR_942606.1:n.380G>T
XM_006715586.3:c.169G>T	XP_006715649.1:p.Glu57Ter
XM_011536196.3:c.358G>T	XP_011534498.1:p.Glu120Ter
XM_011536198.3:c.169G>T	XP_011534500.1:p.Glu57Ter
XM_024446573.1:c.379G>T	XP_024302341.1:p.Glu127Ter
XR_001743697.2:n.460G>T
XR_942606.2:n.511G>T
NM_032861.4:c.379G>T MANE Select	NP_116250.3:p.Glu127Ter
NR_073096.2:n.503G>T