Canonical Allele Identifier: CA366264667

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567873T>G (hg19) ; chr6:g.158146841T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146841T>G , CM000668.2:g.158146841T>G	GRCh38
NC_000006.11:g.158567873T>G , CM000668.1:g.158567873T>G	GRCh37
NC_000006.10:g.158487861T>G	NCBI36
NG_032889.1:g.26440A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*262A>C	ENSP00000475855.1:n.*262A>C
ENST00000642244.1:c.338A>C	ENSP00000493554.1:p.Asp113Ala
ENST00000642903.1:c.428A>C	ENSP00000493559.1:p.Asp143Ala
ENST00000644972.1:c.428A>C	ENSP00000496451.1:p.Asp143Ala
ENST00000645077.1:c.*262A>C	ENSP00000496113.1:n.*262A>C
ENST00000645172.1:c.*189+2024A>C	ENSP00000495367.1:n.*189+2024A>C
ENST00000646190.1:n.1659A>C
ENST00000646208.1:c.164A>C	ENSP00000493723.1:p.Asp55Ala
ENST00000646410.1:c.299A>C	ENSP00000494205.1:p.Asp100Ala
ENST00000646562.1:c.*262A>C	ENSP00000496087.1:n.*262A>C
ENST00000647468.2:c.428A>C MANE Select	ENSP00000496731.1:p.Asp143Ala
ENST00000648111.1:c.*72A>C	ENSP00000497275.1:n.*72A>C
ENST00000367101.5:c.428A>C	ENSP00000356068.1:p.Asp143Ala
ENST00000367104.7:c.428A>C	ENSP00000356071.3:p.Asp143Ala
ENST00000606965.5:c.428A>C	ENSP00000475808.1:p.Asp143Ala
ENST00000607000.1:c.428A>C	ENSP00000475788.1:p.Asp143Ala
ENST00000607071.5:c.*262A>C	ENSP00000475855.1:n.*262A>C
ENST00000607742.5:c.*262A>C	ENSP00000475523.1:n.*262A>C
NM_032861.3:c.428A>C	NP_116250.3:p.Asp143Ala
NR_073096.1:n.570A>C
XM_006715586.1:c.218A>C	XP_006715649.1:p.Asp73Ala
XM_011536196.1:c.407A>C	XP_011534498.1:p.Asp136Ala
XM_011536197.1:c.428A>C	XP_011534499.1:p.Asp143Ala
XM_011536198.1:c.218A>C	XP_011534500.1:p.Asp73Ala
XR_942606.1:n.429A>C
XM_006715586.3:c.218A>C	XP_006715649.1:p.Asp73Ala
XM_011536196.3:c.407A>C	XP_011534498.1:p.Asp136Ala
XM_011536198.3:c.218A>C	XP_011534500.1:p.Asp73Ala
XM_024446573.1:c.428A>C	XP_024302341.1:p.Asp143Ala
XR_001743697.2:n.509A>C
XR_942606.2:n.560A>C
NM_032861.4:c.428A>C MANE Select	NP_116250.3:p.Asp143Ala
NR_073096.2:n.552A>C