Canonical Allele Identifier: CA1562886207

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755110_90755114delinsTTATG , CM000667.2:g.90755110_90755114delinsTTATG	GRCh38
NC_000005.9:g.90050927_90050931delinsTTATG , CM000667.1:g.90050927_90050931delinsTTATG	GRCh37
NC_000005.8:g.90086683_90086687delinsTTATG	NCBI36
NG_007083.1:g.201311_201315delinsTTATG
NG_007083.2:g.230767_230771delinsTTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11505_11509delinsTTATG MANE Select	ENSP00000384582.2:p.Asp3835=
ENST00000425867.3:c.636_640delinsTTATG	ENSP00000392618.3:p.Asp212=
ENST00000639431.1:c.265+78901_265+78905delinsTTATG	ENSP00000491057.1:n.265+78901_265+78905delinsTTATG
ENST00000640374.1:n.4649_4653delinsTTATG
ENST00000640464.1:n.1924_1928delinsTTATG
ENST00000405460.6:c.11505_11509delinsTTATG	ENSP00000384582.2:p.Asp3835=
ENST00000509621.1:c.4202_4206delinsTTATG
NM_032119.3:c.11505_11509delinsTTATG	NP_115495.3:p.Asp3835=
NR_003149.1:n.11518_11522delinsTTATG
XM_011543675.1:c.11502_11506delinsTTATG	XP_011541977.1:p.Asp3834=
XM_011543676.1:c.11424_11428delinsTTATG	XP_011541978.1:p.Asp3808=
XM_011543677.1:c.8808_8812delinsTTATG	XP_011541979.1:p.Asp2936=
XM_011543678.1:c.11505_11509delinsTTATG	XP_011541980.1:p.Asp3835=
NM_032119.4:c.11505_11509delinsTTATG MANE Select	NP_115495.3:p.Asp3835=
XM_017009963.2:c.11526_11530delinsTTATG	XP_016865452.1:p.Asp3842=
XM_017009964.2:c.11523_11527delinsTTATG	XP_016865453.1:p.Asp3841=
XM_017009965.1:c.11523_11527delinsTTATG	XP_016865454.1:p.Asp3841=
XM_017009966.2:c.11445_11449delinsTTATG	XP_016865455.1:p.Asp3815=
XM_017009967.1:c.11430_11434delinsTTATG	XP_016865456.1:p.Asp3810=
XM_017009968.2:c.11526_11530delinsTTATG	XP_016865457.1:p.Asp3842=
XM_017009969.2:c.11526_11530delinsTTATG	XP_016865458.1:p.Asp3842=
XM_017009970.2:c.11526_11530delinsTTATG	XP_016865459.1:p.Asp3842=
XM_017009971.2:c.11526_11530delinsTTATG	XP_016865460.1:p.Asp3842=
XM_017009972.1:c.4644_4648delinsTTATG	XP_016865461.1:p.Asp1548=
XM_017009973.1:c.4623_4627delinsTTATG	XP_016865462.1:p.Asp1541=
NR_003149.2:n.11521_11525delinsTTATG