Canonical Allele Identifier: CA366255259

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535986T>G (hg19) ; chr6:g.158114954T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114954T>G , CM000668.2:g.158114954T>G	GRCh38
NC_000006.11:g.158535986T>G , CM000668.1:g.158535986T>G	GRCh37
NC_000006.10:g.158455974T>G	NCBI36
NG_032889.1:g.58327A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.731A>C	ENSP00000391168.2:n.731A>C
ENST00000607071.6:c.*1239A>C	ENSP00000475855.1:n.*1239A>C
ENST00000642244.1:c.1429A>C	ENSP00000493554.1:p.Met477Leu
ENST00000642903.1:c.1519A>C	ENSP00000493559.1:p.Met507Leu
ENST00000644972.1:c.1519A>C	ENSP00000496451.1:p.Met507Leu
ENST00000645077.1:c.*1140A>C	ENSP00000496113.1:n.*1140A>C
ENST00000645172.1:c.*1221A>C	ENSP00000495367.1:n.*1221A>C
ENST00000646190.1:n.2850A>C
ENST00000646208.1:c.1255A>C	ENSP00000493723.1:p.Met419Leu
ENST00000646410.1:c.1390A>C	ENSP00000494205.1:p.Met464Leu
ENST00000646562.1:c.*1353A>C	ENSP00000496087.1:n.*1353A>C
ENST00000647468.2:c.1519A>C MANE Select	ENSP00000496731.1:p.Met507Leu
ENST00000648111.1:c.*1207A>C	ENSP00000497275.1:n.*1207A>C
ENST00000367101.5:c.1563A>C	ENSP00000356068.1:p.Arg521Ser
ENST00000367104.7:c.1519A>C	ENSP00000356071.3:p.Met507Leu
ENST00000435180.5:c.244A>C	ENSP00000391168.1:p.Met82Leu
ENST00000606965.5:c.*80A>C	ENSP00000475808.1:n.*80A>C
ENST00000607071.5:c.*1453A>C	ENSP00000475855.1:n.*1453A>C
ENST00000607742.5:c.*2797A>C	ENSP00000475523.1:n.*2797A>C
NM_032861.3:c.1519A>C	NP_116250.3:p.Met507Leu
NR_073096.1:n.1452A>C
XM_006715586.1:c.1309A>C	XP_006715649.1:p.Met437Leu
XM_011536196.1:c.1498A>C	XP_011534498.1:p.Met500Leu
XM_011536197.1:c.1405A>C	XP_011534499.1:p.Met469Leu
XM_011536198.1:c.1309A>C	XP_011534500.1:p.Met437Leu
XM_006715586.3:c.1309A>C	XP_006715649.1:p.Met437Leu
XM_011536196.3:c.1498A>C	XP_011534498.1:p.Met500Leu
XM_011536198.3:c.1309A>C	XP_011534500.1:p.Met437Leu
XM_024446573.1:c.1519A>C	XP_024302341.1:p.Met507Leu
XR_001743697.2:n.1550A>C
XR_942606.2:n.1601A>C
NM_032861.4:c.1519A>C MANE Select	NP_116250.3:p.Met507Leu
NR_073096.2:n.1434A>C