Canonical Allele Identifier: CA560901680

Gene: ADGRV1

Linked Data

• gnomAD v2: 5-90021498-GGT-G
• gnomAD v4: 5-90725681-GGT-G
• MyVariant Identifiers: chr5:g.90021499_90021500del (hg19) ; chr5:g.90725682_90725683del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725682_90725683del , CM000667.2:g.90725682_90725683del	GRCh38
NC_000005.9:g.90021499_90021500del , CM000667.1:g.90021499_90021500del	GRCh37
NC_000005.8:g.90057255_90057256del	NCBI36
NG_007083.1:g.171883_171884del
NG_007083.2:g.201339_201340del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+26_10161+27del MANE Select	ENSP00000384582.2:n.10161+26_10161+27del
ENST00000639431.1:c.265+49473_265+49474del	ENSP00000491057.1:n.265+49473_265+49474del
ENST00000640374.1:n.3305+26_3305+27del
ENST00000640464.1:n.580+26_580+27del
ENST00000405460.6:c.10161+26_10161+27del	ENSP00000384582.2:n.10161+26_10161+27del
ENST00000509621.1:c.2858+26_2858+27del
NM_032119.3:c.10161+26_10161+27del	NP_115495.3:n.10161+26_10161+27del
NR_003149.1:n.10174+26_10174+27del
XM_011543675.1:c.10158+26_10158+27del	XP_011541977.1:n.10158+26_10158+27del
XM_011543676.1:c.10080+26_10080+27del	XP_011541978.1:n.10080+26_10080+27del
XM_011543677.1:c.7464+26_7464+27del	XP_011541979.1:n.7464+26_7464+27del
XM_011543678.1:c.10161+26_10161+27del	XP_011541980.1:n.10161+26_10161+27del
XM_011543679.1:c.10161+26_10161+27del	XP_011541981.1:n.10161+26_10161+27del
XR_948560.1:n.272-9874_272-9873del
NM_032119.4:c.10161+26_10161+27del MANE Select	NP_115495.3:n.10161+26_10161+27del
XM_017009963.2:c.10182+26_10182+27del	XP_016865452.1:n.10182+26_10182+27del
XM_017009964.2:c.10179+26_10179+27del	XP_016865453.1:n.10179+26_10179+27del
XM_017009965.1:c.10179+26_10179+27del	XP_016865454.1:n.10179+26_10179+27del
XM_017009966.2:c.10101+26_10101+27del	XP_016865455.1:n.10101+26_10101+27del
XM_017009967.1:c.10086+26_10086+27del	XP_016865456.1:n.10086+26_10086+27del
XM_017009968.2:c.10182+26_10182+27del	XP_016865457.1:n.10182+26_10182+27del
XM_017009969.2:c.10182+26_10182+27del	XP_016865458.1:n.10182+26_10182+27del
XM_017009970.2:c.10182+26_10182+27del	XP_016865459.1:n.10182+26_10182+27del
XM_017009971.2:c.10182+26_10182+27del	XP_016865460.1:n.10182+26_10182+27del
XM_017009972.1:c.3300+26_3300+27del	XP_016865461.1:n.3300+26_3300+27del
XM_017009973.1:c.3279+26_3279+27del	XP_016865462.1:n.3279+26_3279+27del
XM_017009974.2:c.10182+26_10182+27del	XP_016865463.1:n.10182+26_10182+27del
XR_001742802.1:n.2523-9874_2523-9873del
NR_003149.2:n.10177+26_10177+27del