Canonical Allele Identifier: CA16518625

Gene: ATF7IP2

Linked Data

• dbSNP Id: rs13335336
• gnomAD v2: 16-10559263-A-G
• gnomAD v3: 16-10465406-A-G
• gnomAD v4: 16-10465406-A-G
• MyVariant Identifiers: chr16:g.10559263A>G (hg19) ; chr16:g.10465406A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10465406A>G , CM000678.2:g.10465406A>G	GRCh38
NC_000016.9:g.10559263A>G , CM000678.1:g.10559263A>G	GRCh37
NC_000016.8:g.10466764A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000562102.6:c.1353-6704A>G MANE Select	ENSP00000457731.2:n.1353-6704A>G
ENST00000324570.9:c.1353-6704A>G	ENSP00000322811.5:n.1353-6704A>G
ENST00000356427.2:c.1353-6704A>G	ENSP00000348799.2:n.1353-6704A>G
ENST00000396559.5:c.1353-6704A>G	ENSP00000379807.1:n.1353-6704A>G
ENST00000396560.6:c.1353-6704A>G	ENSP00000379808.2:n.1353-6704A>G
ENST00000535850.5:c.1195-8073A>G	ENSP00000440791.1:n.1195-8073A>G
ENST00000543967.5:c.-16-6704A>G	ENSP00000446119.1:n.-16-6704A>G
ENST00000568027.5:c.1195-6704A>G	ENSP00000455259.1:n.1195-6704A>G
NM_001256160.1:c.1353-6704A>G	NP_001243089.1:n.1353-6704A>G
NM_024997.3:c.1353-6704A>G	NP_079273.2:n.1353-6704A>G
NR_045815.1:n.1354-6704A>G
NR_045816.1:n.1422-8073A>G
XM_006720953.2:c.1353-6704A>G	XP_006721016.1:n.1353-6704A>G
XM_011522666.1:c.189-6704A>G	XP_011520968.1:n.189-6704A>G
NM_001256160.2:c.1353-6704A>G	NP_001243089.1:n.1353-6704A>G
NM_001352120.1:c.1353-6704A>G	NP_001339049.1:n.1353-6704A>G
NM_024997.4:c.1353-6704A>G	NP_079273.2:n.1353-6704A>G
NR_045815.2:n.1478-6704A>G
NR_045816.2:n.1478-8073A>G
NR_147927.1:n.1521-6704A>G
XM_006720953.3:c.1353-6704A>G	XP_006721016.1:n.1353-6704A>G
XM_011522666.2:c.189-6704A>G	XP_011520968.1:n.189-6704A>G
XM_017023705.2:c.1353-6704A>G	XP_016879194.1:n.1353-6704A>G
XM_017023706.2:c.1353-6704A>G	XP_016879195.1:n.1353-6704A>G
XM_017023707.2:c.1352+7877A>G	XP_016879196.1:n.1352+7877A>G
XM_017023708.1:c.498-6704A>G	XP_016879197.1:n.498-6704A>G
XM_017023709.1:c.189-6704A>G	XP_016879198.1:n.189-6704A>G
XM_017023710.1:c.186-6704A>G	XP_016879199.1:n.186-6704A>G
XM_017023711.1:c.15-6704A>G	XP_016879200.1:n.15-6704A>G
XR_001751990.1:n.2546+7877A>G
XR_001751991.1:n.1612+7877A>G
XR_001751992.2:n.2388-8073A>G
NM_001256160.3:c.1353-6704A>G	NP_001243089.1:n.1353-6704A>G
NM_001352120.2:c.1353-6704A>G	NP_001339049.1:n.1353-6704A>G
NM_024997.5:c.1353-6704A>G	NP_079273.2:n.1353-6704A>G
NR_045815.3:n.1416-6704A>G
NR_045816.3:n.1416-8073A>G
NR_147927.2:n.1459-6704A>G
NM_001393719.1:c.1353-6704A>G MANE Select	NP_001380648.1:n.1353-6704A>G