Canonical Allele Identifier: CA366255030

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535890A>T (hg19) ; chr6:g.158114858A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114858A>T , CM000668.2:g.158114858A>T	GRCh38
NC_000006.11:g.158535890A>T , CM000668.1:g.158535890A>T	GRCh37
NC_000006.10:g.158455878A>T	NCBI36
NG_032889.1:g.58423T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.827T>A	ENSP00000391168.2:n.827T>A
ENST00000607071.6:c.*1335T>A	ENSP00000475855.1:n.*1335T>A
ENST00000642244.1:c.1525T>A	ENSP00000493554.1:p.Leu509Met
ENST00000642903.1:c.1615T>A	ENSP00000493559.1:p.Leu539Met
ENST00000644972.1:c.1615T>A	ENSP00000496451.1:p.Leu539Met
ENST00000645077.1:c.*1236T>A	ENSP00000496113.1:n.*1236T>A
ENST00000645172.1:c.*1317T>A	ENSP00000495367.1:n.*1317T>A
ENST00000646190.1:n.2946T>A
ENST00000646208.1:c.1351T>A	ENSP00000493723.1:p.Leu451Met
ENST00000646410.1:c.1486T>A	ENSP00000494205.1:p.Leu496Met
ENST00000646562.1:c.*1449T>A	ENSP00000496087.1:n.*1449T>A
ENST00000647468.2:c.1615T>A MANE Select	ENSP00000496731.1:p.Leu539Met
ENST00000648111.1:c.*1303T>A	ENSP00000497275.1:n.*1303T>A
ENST00000367101.5:c.*63T>A	ENSP00000356068.1:n.*63T>A
ENST00000367104.7:c.1615T>A	ENSP00000356071.3:p.Leu539Met
ENST00000435180.5:c.340T>A	ENSP00000391168.1:p.Leu114Met
ENST00000606965.5:c.*176T>A	ENSP00000475808.1:n.*176T>A
ENST00000607071.5:c.*1549T>A	ENSP00000475855.1:n.*1549T>A
ENST00000607742.5:c.*2893T>A	ENSP00000475523.1:n.*2893T>A
NM_032861.3:c.1615T>A	NP_116250.3:p.Leu539Met
NR_073096.1:n.1548T>A
XM_006715586.1:c.1405T>A	XP_006715649.1:p.Leu469Met
XM_011536196.1:c.1594T>A	XP_011534498.1:p.Leu532Met
XM_011536197.1:c.1501T>A	XP_011534499.1:p.Leu501Met
XM_011536198.1:c.1405T>A	XP_011534500.1:p.Leu469Met
XM_006715586.3:c.1405T>A	XP_006715649.1:p.Leu469Met
XM_011536196.3:c.1594T>A	XP_011534498.1:p.Leu532Met
XM_011536198.3:c.1405T>A	XP_011534500.1:p.Leu469Met
XM_024446573.1:c.1615T>A	XP_024302341.1:p.Leu539Met
XR_001743697.2:n.1646T>A
XR_942606.2:n.1697T>A
NM_032861.4:c.1615T>A MANE Select	NP_116250.3:p.Leu539Met
NR_073096.2:n.1530T>A