Canonical Allele Identifier: CA366255126

Gene: SERAC1

Linked Data

• dbSNP Id: rs1275094831
• MyVariant Identifiers: chr6:g.158535935T>C (hg19) ; chr6:g.158114903T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114903T>C , CM000668.2:g.158114903T>C	GRCh38
NC_000006.11:g.158535935T>C , CM000668.1:g.158535935T>C	GRCh37
NC_000006.10:g.158455923T>C	NCBI36
NG_032889.1:g.58378A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.782A>G	ENSP00000391168.2:n.782A>G
ENST00000607071.6:c.*1290A>G	ENSP00000475855.1:n.*1290A>G
ENST00000642244.1:c.1480A>G	ENSP00000493554.1:p.Thr494Ala
ENST00000642903.1:c.1570A>G	ENSP00000493559.1:p.Thr524Ala
ENST00000644972.1:c.1570A>G	ENSP00000496451.1:p.Thr524Ala
ENST00000645077.1:c.*1191A>G	ENSP00000496113.1:n.*1191A>G
ENST00000645172.1:c.*1272A>G	ENSP00000495367.1:n.*1272A>G
ENST00000646190.1:n.2901A>G
ENST00000646208.1:c.1306A>G	ENSP00000493723.1:p.Thr436Ala
ENST00000646410.1:c.1441A>G	ENSP00000494205.1:p.Thr481Ala
ENST00000646562.1:c.*1404A>G	ENSP00000496087.1:n.*1404A>G
ENST00000647468.2:c.1570A>G MANE Select	ENSP00000496731.1:p.Thr524Ala
ENST00000648111.1:c.*1258A>G	ENSP00000497275.1:n.*1258A>G
ENST00000367101.5:c.*18A>G	ENSP00000356068.1:n.*18A>G
ENST00000367104.7:c.1570A>G	ENSP00000356071.3:p.Thr524Ala
ENST00000435180.5:c.295A>G	ENSP00000391168.1:p.Thr99Ala
ENST00000606965.5:c.*131A>G	ENSP00000475808.1:n.*131A>G
ENST00000607071.5:c.*1504A>G	ENSP00000475855.1:n.*1504A>G
ENST00000607742.5:c.*2848A>G	ENSP00000475523.1:n.*2848A>G
NM_032861.3:c.1570A>G	NP_116250.3:p.Thr524Ala
NR_073096.1:n.1503A>G
XM_006715586.1:c.1360A>G	XP_006715649.1:p.Thr454Ala
XM_011536196.1:c.1549A>G	XP_011534498.1:p.Thr517Ala
XM_011536197.1:c.1456A>G	XP_011534499.1:p.Thr486Ala
XM_011536198.1:c.1360A>G	XP_011534500.1:p.Thr454Ala
XM_006715586.3:c.1360A>G	XP_006715649.1:p.Thr454Ala
XM_011536196.3:c.1549A>G	XP_011534498.1:p.Thr517Ala
XM_011536198.3:c.1360A>G	XP_011534500.1:p.Thr454Ala
XM_024446573.1:c.1570A>G	XP_024302341.1:p.Thr524Ala
XR_001743697.2:n.1601A>G
XR_942606.2:n.1652A>G
NM_032861.4:c.1570A>G MANE Select	NP_116250.3:p.Thr524Ala
NR_073096.2:n.1485A>G