Canonical Allele Identifier: CA366255084

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535917A>C (hg19) ; chr6:g.158114885A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114885A>C , CM000668.2:g.158114885A>C	GRCh38
NC_000006.11:g.158535917A>C , CM000668.1:g.158535917A>C	GRCh37
NC_000006.10:g.158455905A>C	NCBI36
NG_032889.1:g.58396T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.800T>G	ENSP00000391168.2:n.800T>G
ENST00000607071.6:c.*1308T>G	ENSP00000475855.1:n.*1308T>G
ENST00000642244.1:c.1498T>G	ENSP00000493554.1:p.Tyr500Asp
ENST00000642903.1:c.1588T>G	ENSP00000493559.1:p.Tyr530Asp
ENST00000644972.1:c.1588T>G	ENSP00000496451.1:p.Tyr530Asp
ENST00000645077.1:c.*1209T>G	ENSP00000496113.1:n.*1209T>G
ENST00000645172.1:c.*1290T>G	ENSP00000495367.1:n.*1290T>G
ENST00000646190.1:n.2919T>G
ENST00000646208.1:c.1324T>G	ENSP00000493723.1:p.Tyr442Asp
ENST00000646410.1:c.1459T>G	ENSP00000494205.1:p.Tyr487Asp
ENST00000646562.1:c.*1422T>G	ENSP00000496087.1:n.*1422T>G
ENST00000647468.2:c.1588T>G MANE Select	ENSP00000496731.1:p.Tyr530Asp
ENST00000648111.1:c.*1276T>G	ENSP00000497275.1:n.*1276T>G
ENST00000367101.5:c.*36T>G	ENSP00000356068.1:n.*36T>G
ENST00000367104.7:c.1588T>G	ENSP00000356071.3:p.Tyr530Asp
ENST00000435180.5:c.313T>G	ENSP00000391168.1:p.Tyr105Asp
ENST00000606965.5:c.*149T>G	ENSP00000475808.1:n.*149T>G
ENST00000607071.5:c.*1522T>G	ENSP00000475855.1:n.*1522T>G
ENST00000607742.5:c.*2866T>G	ENSP00000475523.1:n.*2866T>G
NM_032861.3:c.1588T>G	NP_116250.3:p.Tyr530Asp
NR_073096.1:n.1521T>G
XM_006715586.1:c.1378T>G	XP_006715649.1:p.Tyr460Asp
XM_011536196.1:c.1567T>G	XP_011534498.1:p.Tyr523Asp
XM_011536197.1:c.1474T>G	XP_011534499.1:p.Tyr492Asp
XM_011536198.1:c.1378T>G	XP_011534500.1:p.Tyr460Asp
XM_006715586.3:c.1378T>G	XP_006715649.1:p.Tyr460Asp
XM_011536196.3:c.1567T>G	XP_011534498.1:p.Tyr523Asp
XM_011536198.3:c.1378T>G	XP_011534500.1:p.Tyr460Asp
XM_024446573.1:c.1588T>G	XP_024302341.1:p.Tyr530Asp
XR_001743697.2:n.1619T>G
XR_942606.2:n.1670T>G
NM_032861.4:c.1588T>G MANE Select	NP_116250.3:p.Tyr530Asp
NR_073096.2:n.1503T>G