Canonical Allele Identifier: CA366266801

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158571566C>A (hg19) ; chr6:g.158150534C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158150534C>A , CM000668.2:g.158150534C>A	GRCh38
NC_000006.11:g.158571566C>A , CM000668.1:g.158571566C>A	GRCh37
NC_000006.10:g.158491554C>A	NCBI36
NG_032889.1:g.22747G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*18G>T	ENSP00000475855.1:n.*18G>T
ENST00000642244.1:c.184G>T	ENSP00000493554.1:p.Asp62Tyr
ENST00000642903.1:c.184G>T	ENSP00000493559.1:p.Asp62Tyr
ENST00000643093.1:n.234G>T
ENST00000644972.1:c.184G>T	ENSP00000496451.1:p.Asp62Tyr
ENST00000645077.1:c.*18G>T	ENSP00000496113.1:n.*18G>T
ENST00000645172.1:c.*18G>T	ENSP00000495367.1:n.*18G>T
ENST00000646190.1:n.1415G>T
ENST00000646208.1:c.92-3621G>T	ENSP00000493723.1:n.92-3621G>T
ENST00000646410.1:c.145G>T	ENSP00000494205.1:p.Asp49Tyr
ENST00000646562.1:c.*18G>T	ENSP00000496087.1:n.*18G>T
ENST00000647468.2:c.184G>T MANE Select	ENSP00000496731.1:p.Asp62Tyr
ENST00000648111.1:c.158G>T	ENSP00000497275.1:p.Arg53Ile
ENST00000367101.5:c.184G>T	ENSP00000356068.1:p.Asp62Tyr
ENST00000367104.7:c.184G>T	ENSP00000356071.3:p.Asp62Tyr
ENST00000606965.5:c.184G>T	ENSP00000475808.1:p.Asp62Tyr
ENST00000607000.1:c.184G>T	ENSP00000475788.1:p.Asp62Tyr
ENST00000607071.5:c.*18G>T	ENSP00000475855.1:n.*18G>T
ENST00000607742.5:c.*18G>T	ENSP00000475523.1:n.*18G>T
NM_032861.3:c.184G>T	NP_116250.3:p.Asp62Tyr
NR_073096.1:n.326G>T
XM_006715586.1:c.-27G>T	XP_006715649.1:n.-27G>T
XM_011536196.1:c.163G>T	XP_011534498.1:p.Asp55Tyr
XM_011536197.1:c.184G>T	XP_011534499.1:p.Asp62Tyr
XM_011536198.1:c.-27G>T	XP_011534500.1:n.-27G>T
XR_942606.1:n.185G>T
XM_006715586.3:c.-27G>T	XP_006715649.1:n.-27G>T
XM_011536196.3:c.163G>T	XP_011534498.1:p.Asp55Tyr
XM_011536198.3:c.-27G>T	XP_011534500.1:n.-27G>T
XM_024446573.1:c.184G>T	XP_024302341.1:p.Asp62Tyr
XR_001743697.2:n.265G>T
XR_942606.2:n.316G>T
NM_032861.4:c.184G>T MANE Select	NP_116250.3:p.Asp62Tyr
NR_073096.2:n.308G>T