Canonical Allele Identifier: CA2767408143

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725669_90725670del , CM000667.2:g.90725669_90725670del	GRCh38
NC_000005.9:g.90021486_90021487del , CM000667.1:g.90021486_90021487del	GRCh37
NC_000005.8:g.90057242_90057243del	NCBI36
NG_007083.1:g.171870_171871del
NG_007083.2:g.201326_201327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+13_10161+14del MANE Select	ENSP00000384582.2:n.10161+13_10161+14del
ENST00000639431.1:c.265+49460_265+49461del	ENSP00000491057.1:n.265+49460_265+49461del
ENST00000640374.1:n.3305+13_3305+14del
ENST00000640464.1:n.580+13_580+14del
ENST00000405460.6:c.10161+13_10161+14del	ENSP00000384582.2:n.10161+13_10161+14del
ENST00000509621.1:c.2858+13_2858+14del
NM_032119.3:c.10161+13_10161+14del	NP_115495.3:n.10161+13_10161+14del
NR_003149.1:n.10174+13_10174+14del
XM_011543675.1:c.10158+13_10158+14del	XP_011541977.1:n.10158+13_10158+14del
XM_011543676.1:c.10080+13_10080+14del	XP_011541978.1:n.10080+13_10080+14del
XM_011543677.1:c.7464+13_7464+14del	XP_011541979.1:n.7464+13_7464+14del
XM_011543678.1:c.10161+13_10161+14del	XP_011541980.1:n.10161+13_10161+14del
XM_011543679.1:c.10161+13_10161+14del	XP_011541981.1:n.10161+13_10161+14del
XR_948560.1:n.272-9861_272-9860del
NM_032119.4:c.10161+13_10161+14del MANE Select	NP_115495.3:n.10161+13_10161+14del
XM_017009963.2:c.10182+13_10182+14del	XP_016865452.1:n.10182+13_10182+14del
XM_017009964.2:c.10179+13_10179+14del	XP_016865453.1:n.10179+13_10179+14del
XM_017009965.1:c.10179+13_10179+14del	XP_016865454.1:n.10179+13_10179+14del
XM_017009966.2:c.10101+13_10101+14del	XP_016865455.1:n.10101+13_10101+14del
XM_017009967.1:c.10086+13_10086+14del	XP_016865456.1:n.10086+13_10086+14del
XM_017009968.2:c.10182+13_10182+14del	XP_016865457.1:n.10182+13_10182+14del
XM_017009969.2:c.10182+13_10182+14del	XP_016865458.1:n.10182+13_10182+14del
XM_017009970.2:c.10182+13_10182+14del	XP_016865459.1:n.10182+13_10182+14del
XM_017009971.2:c.10182+13_10182+14del	XP_016865460.1:n.10182+13_10182+14del
XM_017009972.1:c.3300+13_3300+14del	XP_016865461.1:n.3300+13_3300+14del
XM_017009973.1:c.3279+13_3279+14del	XP_016865462.1:n.3279+13_3279+14del
XM_017009974.2:c.10182+13_10182+14del	XP_016865463.1:n.10182+13_10182+14del
XR_001742802.1:n.2523-9861_2523-9860del
NR_003149.2:n.10177+13_10177+14del