Canonical Allele Identifier: CA366255194

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535962G>T (hg19) ; chr6:g.158114930G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114930G>T , CM000668.2:g.158114930G>T	GRCh38
NC_000006.11:g.158535962G>T , CM000668.1:g.158535962G>T	GRCh37
NC_000006.10:g.158455950G>T	NCBI36
NG_032889.1:g.58351C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.755C>A	ENSP00000391168.2:n.755C>A
ENST00000607071.6:c.*1263C>A	ENSP00000475855.1:n.*1263C>A
ENST00000642244.1:c.1453C>A	ENSP00000493554.1:p.Pro485Thr
ENST00000642903.1:c.1543C>A	ENSP00000493559.1:p.Pro515Thr
ENST00000644972.1:c.1543C>A	ENSP00000496451.1:p.Pro515Thr
ENST00000645077.1:c.*1164C>A	ENSP00000496113.1:n.*1164C>A
ENST00000645172.1:c.*1245C>A	ENSP00000495367.1:n.*1245C>A
ENST00000646190.1:n.2874C>A
ENST00000646208.1:c.1279C>A	ENSP00000493723.1:p.Pro427Thr
ENST00000646410.1:c.1414C>A	ENSP00000494205.1:p.Pro472Thr
ENST00000646562.1:c.*1377C>A	ENSP00000496087.1:n.*1377C>A
ENST00000647468.2:c.1543C>A MANE Select	ENSP00000496731.1:p.Pro515Thr
ENST00000648111.1:c.*1231C>A	ENSP00000497275.1:n.*1231C>A
ENST00000367101.5:c.1587C>A	ENSP00000356068.1:p.Ser529Arg
ENST00000367104.7:c.1543C>A	ENSP00000356071.3:p.Pro515Thr
ENST00000435180.5:c.268C>A	ENSP00000391168.1:p.Pro90Thr
ENST00000606965.5:c.*104C>A	ENSP00000475808.1:n.*104C>A
ENST00000607071.5:c.*1477C>A	ENSP00000475855.1:n.*1477C>A
ENST00000607742.5:c.*2821C>A	ENSP00000475523.1:n.*2821C>A
NM_032861.3:c.1543C>A	NP_116250.3:p.Pro515Thr
NR_073096.1:n.1476C>A
XM_006715586.1:c.1333C>A	XP_006715649.1:p.Pro445Thr
XM_011536196.1:c.1522C>A	XP_011534498.1:p.Pro508Thr
XM_011536197.1:c.1429C>A	XP_011534499.1:p.Pro477Thr
XM_011536198.1:c.1333C>A	XP_011534500.1:p.Pro445Thr
XM_006715586.3:c.1333C>A	XP_006715649.1:p.Pro445Thr
XM_011536196.3:c.1522C>A	XP_011534498.1:p.Pro508Thr
XM_011536198.3:c.1333C>A	XP_011534500.1:p.Pro445Thr
XM_024446573.1:c.1543C>A	XP_024302341.1:p.Pro515Thr
XR_001743697.2:n.1574C>A
XR_942606.2:n.1625C>A
NM_032861.4:c.1543C>A MANE Select	NP_116250.3:p.Pro515Thr
NR_073096.2:n.1458C>A