Canonical Allele Identifier: CA366254879

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535821C>G (hg19) ; chr6:g.158114789C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114789C>G , CM000668.2:g.158114789C>G	GRCh38
NC_000006.11:g.158535821C>G , CM000668.1:g.158535821C>G	GRCh37
NC_000006.10:g.158455809C>G	NCBI36
NG_032889.1:g.58492G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404G>C	ENSP00000475855.1:n.*1404G>C
ENST00000642244.1:c.1594G>C	ENSP00000493554.1:p.Asp532His
ENST00000642903.1:c.1684G>C	ENSP00000493559.1:p.Gly562Arg
ENST00000644972.1:c.1684G>C	ENSP00000496451.1:p.Asp562His
ENST00000645077.1:c.*1305G>C	ENSP00000496113.1:n.*1305G>C
ENST00000645172.1:c.*1386G>C	ENSP00000495367.1:n.*1386G>C
ENST00000646190.1:n.3015G>C
ENST00000646208.1:c.1420G>C	ENSP00000493723.1:p.Asp474His
ENST00000646410.1:c.1555G>C	ENSP00000494205.1:p.Asp519His
ENST00000646562.1:c.*1518G>C	ENSP00000496087.1:n.*1518G>C
ENST00000647468.2:c.1684G>C MANE Select	ENSP00000496731.1:p.Asp562His
ENST00000648111.1:c.*1372G>C	ENSP00000497275.1:n.*1372G>C
ENST00000367101.5:c.*132G>C	ENSP00000356068.1:n.*132G>C
ENST00000367104.7:c.1684G>C	ENSP00000356071.3:p.Asp562His
ENST00000435180.5:c.409G>C	ENSP00000391168.1:p.Gly137Arg
ENST00000606965.5:c.*245G>C	ENSP00000475808.1:n.*245G>C
ENST00000607071.5:c.*1618G>C	ENSP00000475855.1:n.*1618G>C
ENST00000607742.5:c.*2962G>C	ENSP00000475523.1:n.*2962G>C
NM_032861.3:c.1684G>C	NP_116250.3:p.Asp562His
NR_073096.1:n.1617G>C
XM_006715586.1:c.1474G>C	XP_006715649.1:p.Asp492His
XM_011536196.1:c.1663G>C	XP_011534498.1:p.Asp555His
XM_011536197.1:c.1570G>C	XP_011534499.1:p.Asp524His
XM_011536198.1:c.1474G>C	XP_011534500.1:p.Asp492His
XM_006715586.3:c.1474G>C	XP_006715649.1:p.Asp492His
XM_011536196.3:c.1663G>C	XP_011534498.1:p.Asp555His
XM_011536198.3:c.1474G>C	XP_011534500.1:p.Asp492His
XM_024446573.1:c.1684G>C	XP_024302341.1:p.Asp562His
XR_001743697.2:n.1715G>C
XR_942606.2:n.1766G>C
NM_032861.4:c.1684G>C MANE Select	NP_116250.3:p.Asp562His
NR_073096.2:n.1599G>C