Canonical Allele Identifier: CA452822195

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567938A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146906A>G , CM000668.2:g.158146906A>G	GRCh38
NC_000006.11:g.158567938A>G , CM000668.1:g.158567938A>G	GRCh37
NC_000006.10:g.158487926A>G	NCBI36
NG_032889.1:g.26375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*197T>C	ENSP00000475855.1:n.*197T>C
ENST00000642244.1:c.273T>C	ENSP00000493554.1:p.Phe91=
ENST00000642903.1:c.363T>C	ENSP00000493559.1:p.Phe121=
ENST00000643093.1:n.413T>C
ENST00000644972.1:c.363T>C	ENSP00000496451.1:p.Phe121=
ENST00000645077.1:c.*197T>C	ENSP00000496113.1:n.*197T>C
ENST00000645172.1:c.*189+1959T>C	ENSP00000495367.1:n.*189+1959T>C
ENST00000646190.1:n.1594T>C
ENST00000646208.1:c.99T>C	ENSP00000493723.1:p.Phe33=
ENST00000646410.1:c.234T>C	ENSP00000494205.1:p.Phe78=
ENST00000646562.1:c.*197T>C	ENSP00000496087.1:n.*197T>C
ENST00000647468.2:c.363T>C MANE Select	ENSP00000496731.1:p.Phe121=
ENST00000648111.1:c.*7T>C	ENSP00000497275.1:n.*7T>C
ENST00000367101.5:c.363T>C	ENSP00000356068.1:p.Phe121=
ENST00000367104.7:c.363T>C	ENSP00000356071.3:p.Phe121=
ENST00000606965.5:c.363T>C	ENSP00000475808.1:p.Phe121=
ENST00000607000.1:c.363T>C	ENSP00000475788.1:p.Phe121=
ENST00000607071.5:c.*197T>C	ENSP00000475855.1:n.*197T>C
ENST00000607742.5:c.*197T>C	ENSP00000475523.1:n.*197T>C
NM_032861.3:c.363T>C	NP_116250.3:p.Phe121=
NR_073096.1:n.505T>C
XM_006715586.1:c.153T>C	XP_006715649.1:p.Phe51=
XM_011536196.1:c.342T>C	XP_011534498.1:p.Phe114=
XM_011536197.1:c.363T>C	XP_011534499.1:p.Phe121=
XM_011536198.1:c.153T>C	XP_011534500.1:p.Phe51=
XR_942606.1:n.364T>C
XM_006715586.3:c.153T>C	XP_006715649.1:p.Phe51=
XM_011536196.3:c.342T>C	XP_011534498.1:p.Phe114=
XM_011536198.3:c.153T>C	XP_011534500.1:p.Phe51=
XM_024446573.1:c.363T>C	XP_024302341.1:p.Phe121=
XR_001743697.2:n.444T>C
XR_942606.2:n.495T>C
NM_032861.4:c.363T>C MANE Select	NP_116250.3:p.Phe121=
NR_073096.2:n.487T>C