Canonical Allele Identifier: CA366266733

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158571551C>G (hg19) ; chr6:g.158150519C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158150519C>G , CM000668.2:g.158150519C>G	GRCh38
NC_000006.11:g.158571551C>G , CM000668.1:g.158571551C>G	GRCh37
NC_000006.10:g.158491539C>G	NCBI36
NG_032889.1:g.22762G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000607071.6:c.*33G>C	ENSP00000475855.1:n.*33G>C
ENST00000642244.1:c.199G>C	ENSP00000493554.1:p.Glu67Gln
ENST00000642903.1:c.199G>C	ENSP00000493559.1:p.Glu67Gln
ENST00000643093.1:n.249G>C
ENST00000644972.1:c.199G>C	ENSP00000496451.1:p.Glu67Gln
ENST00000645077.1:c.*33G>C	ENSP00000496113.1:n.*33G>C
ENST00000645172.1:c.*33G>C	ENSP00000495367.1:n.*33G>C
ENST00000646190.1:n.1430G>C
ENST00000646208.1:c.92-3606G>C	ENSP00000493723.1:n.92-3606G>C
ENST00000646410.1:c.160G>C	ENSP00000494205.1:p.Glu54Gln
ENST00000646562.1:c.*33G>C	ENSP00000496087.1:n.*33G>C
ENST00000647468.2:c.199G>C MANE Select	ENSP00000496731.1:p.Glu67Gln
ENST00000648111.1:c.173G>C	ENSP00000497275.1:p.Arg58Thr
ENST00000367101.5:c.199G>C	ENSP00000356068.1:p.Glu67Gln
ENST00000367104.7:c.199G>C	ENSP00000356071.3:p.Glu67Gln
ENST00000606965.5:c.199G>C	ENSP00000475808.1:p.Glu67Gln
ENST00000607000.1:c.199G>C	ENSP00000475788.1:p.Glu67Gln
ENST00000607071.5:c.*33G>C	ENSP00000475855.1:n.*33G>C
ENST00000607742.5:c.*33G>C	ENSP00000475523.1:n.*33G>C
NM_032861.3:c.199G>C	NP_116250.3:p.Glu67Gln
NR_073096.1:n.341G>C
XM_006715586.1:c.-12G>C	XP_006715649.1:n.-12G>C
XM_011536196.1:c.178G>C	XP_011534498.1:p.Glu60Gln
XM_011536197.1:c.199G>C	XP_011534499.1:p.Glu67Gln
XM_011536198.1:c.-12G>C	XP_011534500.1:n.-12G>C
XR_942606.1:n.200G>C
XM_006715586.3:c.-12G>C	XP_006715649.1:n.-12G>C
XM_011536196.3:c.178G>C	XP_011534498.1:p.Glu60Gln
XM_011536198.3:c.-12G>C	XP_011534500.1:n.-12G>C
XM_024446573.1:c.199G>C	XP_024302341.1:p.Glu67Gln
XR_001743697.2:n.280G>C
XR_942606.2:n.331G>C
NM_032861.4:c.199G>C MANE Select	NP_116250.3:p.Glu67Gln
NR_073096.2:n.323G>C