Canonical Allele Identifier: CA343380959

Gene: ATF6

Linked Data

• MyVariant Identifiers: chr1:g.161823047A>T (hg19) ; chr1:g.161853257A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853257A>T , CM000663.2:g.161853257A>T	GRCh38
NC_000001.10:g.161823047A>T , CM000663.1:g.161823047A>T	GRCh37
NC_000001.9:g.160089671A>T	NCBI36
NG_029773.1:g.92014A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1467A>T MANE Select	ENSP00000356919.3:p.Arg489Ser
ENST00000679833.1:c.1467A>T	ENSP00000505321.1:p.Arg489Ser
ENST00000679853.1:c.1467A>T	ENSP00000506149.1:p.Arg489Ser
ENST00000679886.1:c.861A>T	ENSP00000506559.1:p.Arg287Ser
ENST00000680180.1:n.1507A>T
ENST00000680462.1:c.1467A>T	ENSP00000505583.1:p.Arg489Ser
ENST00000680481.1:c.*1090A>T	ENSP00000505919.1:n.*1090A>T
ENST00000680688.1:c.1524A>T	ENSP00000504865.1:p.Arg508Ser
ENST00000681001.1:c.*1319A>T	ENSP00000506145.1:n.*1319A>T
ENST00000681036.1:c.1269A>T	ENSP00000505474.1:p.Arg423Ser
ENST00000681169.1:c.*385A>T	ENSP00000505455.1:n.*385A>T
ENST00000681187.1:n.1507A>T
ENST00000681492.1:c.1467A>T	ENSP00000506139.1:p.Arg489Ser
ENST00000681541.1:c.1269A>T	ENSP00000506087.1:p.Arg423Ser
ENST00000681557.1:c.*1268A>T	ENSP00000506229.1:n.*1268A>T
ENST00000681738.1:c.1467A>T	ENSP00000505025.1:p.Arg489Ser
ENST00000681779.1:n.1517A>T
ENST00000681801.1:c.1467A>T	ENSP00000505998.1:p.Arg489Ser
ENST00000681912.1:c.1083A>T	ENSP00000505875.1:p.Arg361Ser
ENST00000367942.3:c.1467A>T	ENSP00000356919.3:p.Arg489Ser
ENST00000476437.1:n.674A>T
NM_007348.3:c.1467A>T	NP_031374.2:p.Arg489Ser
XM_006711224.1:c.1467A>T	XP_006711287.1:p.Arg489Ser
XM_011509308.1:c.1524A>T	XP_011507610.1:p.Arg508Ser
XM_011509309.1:c.1524A>T	XP_011507611.1:p.Arg508Ser
XM_011509310.1:c.1524A>T	XP_011507612.1:p.Arg508Ser
XM_011509310.2:c.1524A>T	XP_011507612.1:p.Arg508Ser
NM_007348.4:c.1467A>T MANE Select	NP_031374.2:p.Arg489Ser