Canonical Allele Identifier: CA366255148

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535944T>G (hg19) ; chr6:g.158114912T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114912T>G , CM000668.2:g.158114912T>G	GRCh38
NC_000006.11:g.158535944T>G , CM000668.1:g.158535944T>G	GRCh37
NC_000006.10:g.158455932T>G	NCBI36
NG_032889.1:g.58369A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.773A>C	ENSP00000391168.2:n.773A>C
ENST00000607071.6:c.*1281A>C	ENSP00000475855.1:n.*1281A>C
ENST00000642244.1:c.1471A>C	ENSP00000493554.1:p.Ile491Leu
ENST00000642903.1:c.1561A>C	ENSP00000493559.1:p.Ile521Leu
ENST00000644972.1:c.1561A>C	ENSP00000496451.1:p.Ile521Leu
ENST00000645077.1:c.*1182A>C	ENSP00000496113.1:n.*1182A>C
ENST00000645172.1:c.*1263A>C	ENSP00000495367.1:n.*1263A>C
ENST00000646190.1:n.2892A>C
ENST00000646208.1:c.1297A>C	ENSP00000493723.1:p.Ile433Leu
ENST00000646410.1:c.1432A>C	ENSP00000494205.1:p.Ile478Leu
ENST00000646562.1:c.*1395A>C	ENSP00000496087.1:n.*1395A>C
ENST00000647468.2:c.1561A>C MANE Select	ENSP00000496731.1:p.Ile521Leu
ENST00000648111.1:c.*1249A>C	ENSP00000497275.1:n.*1249A>C
ENST00000367101.5:c.*9A>C	ENSP00000356068.1:n.*9A>C
ENST00000367104.7:c.1561A>C	ENSP00000356071.3:p.Ile521Leu
ENST00000435180.5:c.286A>C	ENSP00000391168.1:p.Ile96Leu
ENST00000606965.5:c.*122A>C	ENSP00000475808.1:n.*122A>C
ENST00000607071.5:c.*1495A>C	ENSP00000475855.1:n.*1495A>C
ENST00000607742.5:c.*2839A>C	ENSP00000475523.1:n.*2839A>C
NM_032861.3:c.1561A>C	NP_116250.3:p.Ile521Leu
NR_073096.1:n.1494A>C
XM_006715586.1:c.1351A>C	XP_006715649.1:p.Ile451Leu
XM_011536196.1:c.1540A>C	XP_011534498.1:p.Ile514Leu
XM_011536197.1:c.1447A>C	XP_011534499.1:p.Ile483Leu
XM_011536198.1:c.1351A>C	XP_011534500.1:p.Ile451Leu
XM_006715586.3:c.1351A>C	XP_006715649.1:p.Ile451Leu
XM_011536196.3:c.1540A>C	XP_011534498.1:p.Ile514Leu
XM_011536198.3:c.1351A>C	XP_011534500.1:p.Ile451Leu
XM_024446573.1:c.1561A>C	XP_024302341.1:p.Ile521Leu
XR_001743697.2:n.1592A>C
XR_942606.2:n.1643A>C
NM_032861.4:c.1561A>C MANE Select	NP_116250.3:p.Ile521Leu
NR_073096.2:n.1476A>C