Canonical Allele Identifier: CA366256759

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158538766T>G (hg19) ; chr6:g.158117734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158117734T>G , CM000668.2:g.158117734T>G	GRCh38
NC_000006.11:g.158538766T>G , CM000668.1:g.158538766T>G	GRCh37
NC_000006.10:g.158458754T>G	NCBI36
NG_032889.1:g.55547A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.608A>C	ENSP00000391168.2:n.608A>C
ENST00000607071.6:c.*1116A>C	ENSP00000475855.1:n.*1116A>C
ENST00000642244.1:c.1306A>C	ENSP00000493554.1:p.Met436Leu
ENST00000642903.1:c.1396A>C	ENSP00000493559.1:p.Met466Leu
ENST00000644972.1:c.1396A>C	ENSP00000496451.1:p.Met466Leu
ENST00000645077.1:c.*1017A>C	ENSP00000496113.1:n.*1017A>C
ENST00000645172.1:c.*1098A>C	ENSP00000495367.1:n.*1098A>C
ENST00000646190.1:n.2727A>C
ENST00000646208.1:c.1132A>C	ENSP00000493723.1:p.Met378Leu
ENST00000646410.1:c.1267A>C	ENSP00000494205.1:p.Met423Leu
ENST00000646562.1:c.*1230A>C	ENSP00000496087.1:n.*1230A>C
ENST00000647468.2:c.1396A>C MANE Select	ENSP00000496731.1:p.Met466Leu
ENST00000648111.1:c.*1040A>C	ENSP00000497275.1:n.*1040A>C
ENST00000367101.5:c.1396A>C	ENSP00000356068.1:p.Met466Leu
ENST00000367104.7:c.1396A>C	ENSP00000356071.3:p.Met466Leu
ENST00000435180.5:c.121A>C	ENSP00000391168.1:p.Met41Leu
ENST00000606965.5:c.1194+1295A>C	ENSP00000475808.1:n.1194+1295A>C
ENST00000607071.5:c.*1330A>C	ENSP00000475855.1:n.*1330A>C
ENST00000607742.5:c.*1230A>C	ENSP00000475523.1:n.*1230A>C
NM_032861.3:c.1396A>C	NP_116250.3:p.Met466Leu
NR_073096.1:n.1336+1295A>C
XM_006715586.1:c.1186A>C	XP_006715649.1:p.Met396Leu
XM_011536196.1:c.1375A>C	XP_011534498.1:p.Met459Leu
XM_011536197.1:c.1282A>C	XP_011534499.1:p.Met428Leu
XM_011536198.1:c.1186A>C	XP_011534500.1:p.Met396Leu
XR_942606.1:n.1347A>C
XM_006715586.3:c.1186A>C	XP_006715649.1:p.Met396Leu
XM_011536196.3:c.1375A>C	XP_011534498.1:p.Met459Leu
XM_011536198.3:c.1186A>C	XP_011534500.1:p.Met396Leu
XM_024446573.1:c.1396A>C	XP_024302341.1:p.Met466Leu
XR_001743697.2:n.1427A>C
XR_942606.2:n.1478A>C
NM_032861.4:c.1396A>C MANE Select	NP_116250.3:p.Met466Leu
NR_073096.2:n.1318+1295A>C