Canonical Allele Identifier: CA2767408151

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725703_90725704del , CM000667.2:g.90725703_90725704del	GRCh38
NC_000005.9:g.90021520_90021521del , CM000667.1:g.90021520_90021521del	GRCh37
NC_000005.8:g.90057276_90057277del	NCBI36
NG_007083.1:g.171904_171905del
NG_007083.2:g.201360_201361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+47_10161+48del MANE Select	ENSP00000384582.2:n.10161+47_10161+48del
ENST00000639431.1:c.265+49494_265+49495del	ENSP00000491057.1:n.265+49494_265+49495del
ENST00000640374.1:n.3305+47_3305+48del
ENST00000640464.1:n.580+47_580+48del
ENST00000405460.6:c.10161+47_10161+48del	ENSP00000384582.2:n.10161+47_10161+48del
ENST00000509621.1:c.2858+47_2858+48del
NM_032119.3:c.10161+47_10161+48del	NP_115495.3:n.10161+47_10161+48del
NR_003149.1:n.10174+47_10174+48del
XM_011543675.1:c.10158+47_10158+48del	XP_011541977.1:n.10158+47_10158+48del
XM_011543676.1:c.10080+47_10080+48del	XP_011541978.1:n.10080+47_10080+48del
XM_011543677.1:c.7464+47_7464+48del	XP_011541979.1:n.7464+47_7464+48del
XM_011543678.1:c.10161+47_10161+48del	XP_011541980.1:n.10161+47_10161+48del
XM_011543679.1:c.10161+47_10161+48del	XP_011541981.1:n.10161+47_10161+48del
XR_948560.1:n.272-9895_272-9894del
NM_032119.4:c.10161+47_10161+48del MANE Select	NP_115495.3:n.10161+47_10161+48del
XM_017009963.2:c.10182+47_10182+48del	XP_016865452.1:n.10182+47_10182+48del
XM_017009964.2:c.10179+47_10179+48del	XP_016865453.1:n.10179+47_10179+48del
XM_017009965.1:c.10179+47_10179+48del	XP_016865454.1:n.10179+47_10179+48del
XM_017009966.2:c.10101+47_10101+48del	XP_016865455.1:n.10101+47_10101+48del
XM_017009967.1:c.10086+47_10086+48del	XP_016865456.1:n.10086+47_10086+48del
XM_017009968.2:c.10182+47_10182+48del	XP_016865457.1:n.10182+47_10182+48del
XM_017009969.2:c.10182+47_10182+48del	XP_016865458.1:n.10182+47_10182+48del
XM_017009970.2:c.10182+47_10182+48del	XP_016865459.1:n.10182+47_10182+48del
XM_017009971.2:c.10182+47_10182+48del	XP_016865460.1:n.10182+47_10182+48del
XM_017009972.1:c.3300+47_3300+48del	XP_016865461.1:n.3300+47_3300+48del
XM_017009973.1:c.3279+47_3279+48del	XP_016865462.1:n.3279+47_3279+48del
XM_017009974.2:c.10182+47_10182+48del	XP_016865463.1:n.10182+47_10182+48del
XR_001742802.1:n.2523-9895_2523-9894del
NR_003149.2:n.10177+47_10177+48del