Canonical Allele Identifier: CA2674548564

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90725698-CTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725700_90725703del , CM000667.2:g.90725700_90725703del	GRCh38
NC_000005.9:g.90021517_90021520del , CM000667.1:g.90021517_90021520del	GRCh37
NC_000005.8:g.90057273_90057276del	NCBI36
NG_007083.1:g.171901_171904del
NG_007083.2:g.201357_201360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+44_10161+47del MANE Select	ENSP00000384582.2:n.10161+44_10161+47del
ENST00000639431.1:c.265+49491_265+49494del	ENSP00000491057.1:n.265+49491_265+49494del
ENST00000640374.1:n.3305+44_3305+47del
ENST00000640464.1:n.580+44_580+47del
ENST00000405460.6:c.10161+44_10161+47del	ENSP00000384582.2:n.10161+44_10161+47del
ENST00000509621.1:c.2858+44_2858+47del
NM_032119.3:c.10161+44_10161+47del	NP_115495.3:n.10161+44_10161+47del
NR_003149.1:n.10174+44_10174+47del
XM_011543675.1:c.10158+44_10158+47del	XP_011541977.1:n.10158+44_10158+47del
XM_011543676.1:c.10080+44_10080+47del	XP_011541978.1:n.10080+44_10080+47del
XM_011543677.1:c.7464+44_7464+47del	XP_011541979.1:n.7464+44_7464+47del
XM_011543678.1:c.10161+44_10161+47del	XP_011541980.1:n.10161+44_10161+47del
XM_011543679.1:c.10161+44_10161+47del	XP_011541981.1:n.10161+44_10161+47del
XR_948560.1:n.272-9893_272-9890del
NM_032119.4:c.10161+44_10161+47del MANE Select	NP_115495.3:n.10161+44_10161+47del
XM_017009963.2:c.10182+44_10182+47del	XP_016865452.1:n.10182+44_10182+47del
XM_017009964.2:c.10179+44_10179+47del	XP_016865453.1:n.10179+44_10179+47del
XM_017009965.1:c.10179+44_10179+47del	XP_016865454.1:n.10179+44_10179+47del
XM_017009966.2:c.10101+44_10101+47del	XP_016865455.1:n.10101+44_10101+47del
XM_017009967.1:c.10086+44_10086+47del	XP_016865456.1:n.10086+44_10086+47del
XM_017009968.2:c.10182+44_10182+47del	XP_016865457.1:n.10182+44_10182+47del
XM_017009969.2:c.10182+44_10182+47del	XP_016865458.1:n.10182+44_10182+47del
XM_017009970.2:c.10182+44_10182+47del	XP_016865459.1:n.10182+44_10182+47del
XM_017009971.2:c.10182+44_10182+47del	XP_016865460.1:n.10182+44_10182+47del
XM_017009972.1:c.3300+44_3300+47del	XP_016865461.1:n.3300+44_3300+47del
XM_017009973.1:c.3279+44_3279+47del	XP_016865462.1:n.3279+44_3279+47del
XM_017009974.2:c.10182+44_10182+47del	XP_016865463.1:n.10182+44_10182+47del
XR_001742802.1:n.2523-9893_2523-9890del
NR_003149.2:n.10177+44_10177+47del