Canonical Allele Identifier: CA366254982

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535869T>A (hg19) ; chr6:g.158114837T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114837T>A , CM000668.2:g.158114837T>A	GRCh38
NC_000006.11:g.158535869T>A , CM000668.1:g.158535869T>A	GRCh37
NC_000006.10:g.158455857T>A	NCBI36
NG_032889.1:g.58444A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.848A>T	ENSP00000391168.2:n.848A>T
ENST00000607071.6:c.*1356A>T	ENSP00000475855.1:n.*1356A>T
ENST00000642244.1:c.1546A>T	ENSP00000493554.1:p.Ile516Phe
ENST00000642903.1:c.1636A>T	ENSP00000493559.1:p.Ile546Phe
ENST00000644972.1:c.1636A>T	ENSP00000496451.1:p.Ile546Phe
ENST00000645077.1:c.*1257A>T	ENSP00000496113.1:n.*1257A>T
ENST00000645172.1:c.*1338A>T	ENSP00000495367.1:n.*1338A>T
ENST00000646190.1:n.2967A>T
ENST00000646208.1:c.1372A>T	ENSP00000493723.1:p.Ile458Phe
ENST00000646410.1:c.1507A>T	ENSP00000494205.1:p.Ile503Phe
ENST00000646562.1:c.*1470A>T	ENSP00000496087.1:n.*1470A>T
ENST00000647468.2:c.1636A>T MANE Select	ENSP00000496731.1:p.Ile546Phe
ENST00000648111.1:c.*1324A>T	ENSP00000497275.1:n.*1324A>T
ENST00000367101.5:c.*84A>T	ENSP00000356068.1:n.*84A>T
ENST00000367104.7:c.1636A>T	ENSP00000356071.3:p.Ile546Phe
ENST00000435180.5:c.361A>T	ENSP00000391168.1:p.Ile121Phe
ENST00000606965.5:c.*197A>T	ENSP00000475808.1:n.*197A>T
ENST00000607071.5:c.*1570A>T	ENSP00000475855.1:n.*1570A>T
ENST00000607742.5:c.*2914A>T	ENSP00000475523.1:n.*2914A>T
NM_032861.3:c.1636A>T	NP_116250.3:p.Ile546Phe
NR_073096.1:n.1569A>T
XM_006715586.1:c.1426A>T	XP_006715649.1:p.Ile476Phe
XM_011536196.1:c.1615A>T	XP_011534498.1:p.Ile539Phe
XM_011536197.1:c.1522A>T	XP_011534499.1:p.Ile508Phe
XM_011536198.1:c.1426A>T	XP_011534500.1:p.Ile476Phe
XM_006715586.3:c.1426A>T	XP_006715649.1:p.Ile476Phe
XM_011536196.3:c.1615A>T	XP_011534498.1:p.Ile539Phe
XM_011536198.3:c.1426A>T	XP_011534500.1:p.Ile476Phe
XM_024446573.1:c.1636A>T	XP_024302341.1:p.Ile546Phe
XR_001743697.2:n.1667A>T
XR_942606.2:n.1718A>T
NM_032861.4:c.1636A>T MANE Select	NP_116250.3:p.Ile546Phe
NR_073096.2:n.1551A>T