Canonical Allele Identifier: CA366265021

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567939A>G (hg19) ; chr6:g.158146907A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146907A>G , CM000668.2:g.158146907A>G	GRCh38
NC_000006.11:g.158567939A>G , CM000668.1:g.158567939A>G	GRCh37
NC_000006.10:g.158487927A>G	NCBI36
NG_032889.1:g.26374T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*196T>C	ENSP00000475855.1:n.*196T>C
ENST00000642244.1:c.272T>C	ENSP00000493554.1:p.Phe91Ser
ENST00000642903.1:c.362T>C	ENSP00000493559.1:p.Phe121Ser
ENST00000643093.1:n.412T>C
ENST00000644972.1:c.362T>C	ENSP00000496451.1:p.Phe121Ser
ENST00000645077.1:c.*196T>C	ENSP00000496113.1:n.*196T>C
ENST00000645172.1:c.*189+1958T>C	ENSP00000495367.1:n.*189+1958T>C
ENST00000646190.1:n.1593T>C
ENST00000646208.1:c.98T>C	ENSP00000493723.1:p.Phe33Ser
ENST00000646410.1:c.233T>C	ENSP00000494205.1:p.Phe78Ser
ENST00000646562.1:c.*196T>C	ENSP00000496087.1:n.*196T>C
ENST00000647468.2:c.362T>C MANE Select	ENSP00000496731.1:p.Phe121Ser
ENST00000648111.1:c.*6T>C	ENSP00000497275.1:n.*6T>C
ENST00000367101.5:c.362T>C	ENSP00000356068.1:p.Phe121Ser
ENST00000367104.7:c.362T>C	ENSP00000356071.3:p.Phe121Ser
ENST00000606965.5:c.362T>C	ENSP00000475808.1:p.Phe121Ser
ENST00000607000.1:c.362T>C	ENSP00000475788.1:p.Phe121Ser
ENST00000607071.5:c.*196T>C	ENSP00000475855.1:n.*196T>C
ENST00000607742.5:c.*196T>C	ENSP00000475523.1:n.*196T>C
NM_032861.3:c.362T>C	NP_116250.3:p.Phe121Ser
NR_073096.1:n.504T>C
XM_006715586.1:c.152T>C	XP_006715649.1:p.Phe51Ser
XM_011536196.1:c.341T>C	XP_011534498.1:p.Phe114Ser
XM_011536197.1:c.362T>C	XP_011534499.1:p.Phe121Ser
XM_011536198.1:c.152T>C	XP_011534500.1:p.Phe51Ser
XR_942606.1:n.363T>C
XM_006715586.3:c.152T>C	XP_006715649.1:p.Phe51Ser
XM_011536196.3:c.341T>C	XP_011534498.1:p.Phe114Ser
XM_011536198.3:c.152T>C	XP_011534500.1:p.Phe51Ser
XM_024446573.1:c.362T>C	XP_024302341.1:p.Phe121Ser
XR_001743697.2:n.443T>C
XR_942606.2:n.494T>C
NM_032861.4:c.362T>C MANE Select	NP_116250.3:p.Phe121Ser
NR_073096.2:n.486T>C