Canonical Allele Identifier: CA366255292

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535998G>C (hg19) ; chr6:g.158114966G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114966G>C , CM000668.2:g.158114966G>C	GRCh38
NC_000006.11:g.158535998G>C , CM000668.1:g.158535998G>C	GRCh37
NC_000006.10:g.158455986G>C	NCBI36
NG_032889.1:g.58315C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.719C>G	ENSP00000391168.2:n.719C>G
ENST00000607071.6:c.*1227C>G	ENSP00000475855.1:n.*1227C>G
ENST00000642244.1:c.1417C>G	ENSP00000493554.1:p.Leu473Val
ENST00000642903.1:c.1507C>G	ENSP00000493559.1:p.Leu503Val
ENST00000644972.1:c.1507C>G	ENSP00000496451.1:p.Leu503Val
ENST00000645077.1:c.*1128C>G	ENSP00000496113.1:n.*1128C>G
ENST00000645172.1:c.*1209C>G	ENSP00000495367.1:n.*1209C>G
ENST00000646190.1:n.2838C>G
ENST00000646208.1:c.1243C>G	ENSP00000493723.1:p.Leu415Val
ENST00000646410.1:c.1378C>G	ENSP00000494205.1:p.Leu460Val
ENST00000646562.1:c.*1341C>G	ENSP00000496087.1:n.*1341C>G
ENST00000647468.2:c.1507C>G MANE Select	ENSP00000496731.1:p.Leu503Val
ENST00000648111.1:c.*1195C>G	ENSP00000497275.1:n.*1195C>G
ENST00000367101.5:c.1551C>G	ENSP00000356068.1:p.Phe517Leu
ENST00000367104.7:c.1507C>G	ENSP00000356071.3:p.Leu503Val
ENST00000435180.5:c.232C>G	ENSP00000391168.1:p.Leu78Val
ENST00000606965.5:c.*68C>G	ENSP00000475808.1:n.*68C>G
ENST00000607071.5:c.*1441C>G	ENSP00000475855.1:n.*1441C>G
ENST00000607742.5:c.*2785C>G	ENSP00000475523.1:n.*2785C>G
NM_032861.3:c.1507C>G	NP_116250.3:p.Leu503Val
NR_073096.1:n.1440C>G
XM_006715586.1:c.1297C>G	XP_006715649.1:p.Leu433Val
XM_011536196.1:c.1486C>G	XP_011534498.1:p.Leu496Val
XM_011536197.1:c.1393C>G	XP_011534499.1:p.Leu465Val
XM_011536198.1:c.1297C>G	XP_011534500.1:p.Leu433Val
XM_006715586.3:c.1297C>G	XP_006715649.1:p.Leu433Val
XM_011536196.3:c.1486C>G	XP_011534498.1:p.Leu496Val
XM_011536198.3:c.1297C>G	XP_011534500.1:p.Leu433Val
XM_024446573.1:c.1507C>G	XP_024302341.1:p.Leu503Val
XR_001743697.2:n.1538C>G
XR_942606.2:n.1589C>G
NM_032861.4:c.1507C>G MANE Select	NP_116250.3:p.Leu503Val
NR_073096.2:n.1422C>G