Canonical Allele Identifier: CA890227152

Gene: ATF6

Linked Data

• dbSNP Id: rs1306885532
• gnomAD v4: 1-161853197-TTTAA-T
• MyVariant Identifiers: chr1:g.161822988_161822991del (hg19) ; chr1:g.161853198_161853201del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161853206_161853209del , CM000663.2:g.161853206_161853209del	GRCh38
NC_000001.10:g.161822996_161822999del , CM000663.1:g.161822996_161822999del	GRCh37
NC_000001.9:g.160089620_160089623del	NCBI36
NG_029773.1:g.91963_91966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367942.4:c.1434-18_1434-15del MANE Select	ENSP00000356919.3:n.1434-18_1434-15del
ENST00000679833.1:c.1434-18_1434-15del	ENSP00000505321.1:n.1434-18_1434-15del
ENST00000679853.1:c.1434-18_1434-15del	ENSP00000506149.1:n.1434-18_1434-15del
ENST00000679886.1:c.828-18_828-15del	ENSP00000506559.1:n.828-18_828-15del
ENST00000680180.1:n.1474-18_1474-15del
ENST00000680462.1:c.1434-18_1434-15del	ENSP00000505583.1:n.1434-18_1434-15del
ENST00000680481.1:c.*1057-18_*1057-15del	ENSP00000505919.1:n.*1057-18_*1057-15del
ENST00000680688.1:c.1491-18_1491-15del	ENSP00000504865.1:n.1491-18_1491-15del
ENST00000681001.1:c.*1286-18_*1286-15del	ENSP00000506145.1:n.*1286-18_*1286-15del
ENST00000681036.1:c.1236-18_1236-15del	ENSP00000505474.1:n.1236-18_1236-15del
ENST00000681169.1:c.*352-18_*352-15del	ENSP00000505455.1:n.*352-18_*352-15del
ENST00000681187.1:n.1474-18_1474-15del
ENST00000681492.1:c.1434-18_1434-15del	ENSP00000506139.1:n.1434-18_1434-15del
ENST00000681541.1:c.1236-18_1236-15del	ENSP00000506087.1:n.1236-18_1236-15del
ENST00000681557.1:c.*1235-18_*1235-15del	ENSP00000506229.1:n.*1235-18_*1235-15del
ENST00000681738.1:c.1434-18_1434-15del	ENSP00000505025.1:n.1434-18_1434-15del
ENST00000681779.1:n.1484-18_1484-15del
ENST00000681801.1:c.1434-18_1434-15del	ENSP00000505998.1:n.1434-18_1434-15del
ENST00000681912.1:c.1050-18_1050-15del	ENSP00000505875.1:n.1050-18_1050-15del
ENST00000367942.3:c.1434-18_1434-15del	ENSP00000356919.3:n.1434-18_1434-15del
ENST00000476437.1:n.641-18_641-15del
NM_007348.3:c.1434-18_1434-15del	NP_031374.2:n.1434-18_1434-15del
XM_006711224.1:c.1434-18_1434-15del	XP_006711287.1:n.1434-18_1434-15del
XM_011509308.1:c.1491-18_1491-15del	XP_011507610.1:n.1491-18_1491-15del
XM_011509309.1:c.1491-18_1491-15del	XP_011507611.1:n.1491-18_1491-15del
XM_011509310.1:c.1491-18_1491-15del	XP_011507612.1:n.1491-18_1491-15del
XM_011509310.2:c.1491-18_1491-15del	XP_011507612.1:n.1491-18_1491-15del
NM_007348.4:c.1434-18_1434-15del MANE Select	NP_031374.2:n.1434-18_1434-15del