Canonical Allele Identifier: CA2767405926

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716764_90716765insAG , CM000667.2:g.90716764_90716765insAG	GRCh38
NC_000005.9:g.90012581_90012582insAG , CM000667.1:g.90012581_90012582insAG	GRCh37
NC_000005.8:g.90048337_90048338insAG	NCBI36
NG_007083.1:g.162965_162966insAG
NG_007083.2:g.192421_192422insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9447+35_9447+36insAG MANE Select	ENSP00000384582.2:n.9447+35_9447+36insAG
ENST00000639431.1:c.265+40555_265+40556insAG	ENSP00000491057.1:n.265+40555_265+40556insAG
ENST00000639473.1:n.4941_4942insAG
ENST00000640374.1:n.2591+35_2591+36insAG
ENST00000640779.1:c.4176+35_4176+36insAG
ENST00000405460.6:c.9447+35_9447+36insAG	ENSP00000384582.2:n.9447+35_9447+36insAG
ENST00000509621.1:c.2144+35_2144+36insAG
NM_032119.3:c.9447+35_9447+36insAG	NP_115495.3:n.9447+35_9447+36insAG
NR_003149.1:n.9460+35_9460+36insAG
XM_011543675.1:c.9444+35_9444+36insAG	XP_011541977.1:n.9444+35_9444+36insAG
XM_011543676.1:c.9366+35_9366+36insAG	XP_011541978.1:n.9366+35_9366+36insAG
XM_011543677.1:c.6750+35_6750+36insAG	XP_011541979.1:n.6750+35_6750+36insAG
XM_011543678.1:c.9447+35_9447+36insAG	XP_011541980.1:n.9447+35_9447+36insAG
XM_011543679.1:c.9447+35_9447+36insAG	XP_011541981.1:n.9447+35_9447+36insAG
XR_948560.1:n.272-956_272-955insCT
NM_032119.4:c.9447+35_9447+36insAG MANE Select	NP_115495.3:n.9447+35_9447+36insAG
XM_017009963.2:c.9468+35_9468+36insAG	XP_016865452.1:n.9468+35_9468+36insAG
XM_017009964.2:c.9465+35_9465+36insAG	XP_016865453.1:n.9465+35_9465+36insAG
XM_017009965.1:c.9465+35_9465+36insAG	XP_016865454.1:n.9465+35_9465+36insAG
XM_017009966.2:c.9387+35_9387+36insAG	XP_016865455.1:n.9387+35_9387+36insAG
XM_017009967.1:c.9372+35_9372+36insAG	XP_016865456.1:n.9372+35_9372+36insAG
XM_017009968.2:c.9468+35_9468+36insAG	XP_016865457.1:n.9468+35_9468+36insAG
XM_017009969.2:c.9468+35_9468+36insAG	XP_016865458.1:n.9468+35_9468+36insAG
XM_017009970.2:c.9468+35_9468+36insAG	XP_016865459.1:n.9468+35_9468+36insAG
XM_017009971.2:c.9468+35_9468+36insAG	XP_016865460.1:n.9468+35_9468+36insAG
XM_017009972.1:c.2586+35_2586+36insAG	XP_016865461.1:n.2586+35_2586+36insAG
XM_017009973.1:c.2565+35_2565+36insAG	XP_016865462.1:n.2565+35_2565+36insAG
XM_017009974.2:c.9468+35_9468+36insAG	XP_016865463.1:n.9468+35_9468+36insAG
XR_001742802.1:n.2523-956_2523-955insCT
NR_003149.2:n.9463+35_9463+36insAG