Canonical Allele Identifier: CA2674548545

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90725681-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725681_90725682insTTTT , CM000667.2:g.90725681_90725682insTTTT	GRCh38
NC_000005.9:g.90021498_90021499insTTTT , CM000667.1:g.90021498_90021499insTTTT	GRCh37
NC_000005.8:g.90057254_90057255insTTTT	NCBI36
NG_007083.1:g.171882_171883insTTTT
NG_007083.2:g.201338_201339insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+25_10161+26insTTTT MANE Select	ENSP00000384582.2:n.10161+25_10161+26insTTTT
ENST00000639431.1:c.265+49472_265+49473insTTTT	ENSP00000491057.1:n.265+49472_265+49473insTTTT
ENST00000640374.1:n.3305+25_3305+26insTTTT
ENST00000640464.1:n.580+25_580+26insTTTT
ENST00000405460.6:c.10161+25_10161+26insTTTT	ENSP00000384582.2:n.10161+25_10161+26insTTTT
ENST00000509621.1:c.2858+25_2858+26insTTTT
NM_032119.3:c.10161+25_10161+26insTTTT	NP_115495.3:n.10161+25_10161+26insTTTT
NR_003149.1:n.10174+25_10174+26insTTTT
XM_011543675.1:c.10158+25_10158+26insTTTT	XP_011541977.1:n.10158+25_10158+26insTTTT
XM_011543676.1:c.10080+25_10080+26insTTTT	XP_011541978.1:n.10080+25_10080+26insTTTT
XM_011543677.1:c.7464+25_7464+26insTTTT	XP_011541979.1:n.7464+25_7464+26insTTTT
XM_011543678.1:c.10161+25_10161+26insTTTT	XP_011541980.1:n.10161+25_10161+26insTTTT
XM_011543679.1:c.10161+25_10161+26insTTTT	XP_011541981.1:n.10161+25_10161+26insTTTT
XR_948560.1:n.272-9873_272-9872insAAAA
NM_032119.4:c.10161+25_10161+26insTTTT MANE Select	NP_115495.3:n.10161+25_10161+26insTTTT
XM_017009963.2:c.10182+25_10182+26insTTTT	XP_016865452.1:n.10182+25_10182+26insTTTT
XM_017009964.2:c.10179+25_10179+26insTTTT	XP_016865453.1:n.10179+25_10179+26insTTTT
XM_017009965.1:c.10179+25_10179+26insTTTT	XP_016865454.1:n.10179+25_10179+26insTTTT
XM_017009966.2:c.10101+25_10101+26insTTTT	XP_016865455.1:n.10101+25_10101+26insTTTT
XM_017009967.1:c.10086+25_10086+26insTTTT	XP_016865456.1:n.10086+25_10086+26insTTTT
XM_017009968.2:c.10182+25_10182+26insTTTT	XP_016865457.1:n.10182+25_10182+26insTTTT
XM_017009969.2:c.10182+25_10182+26insTTTT	XP_016865458.1:n.10182+25_10182+26insTTTT
XM_017009970.2:c.10182+25_10182+26insTTTT	XP_016865459.1:n.10182+25_10182+26insTTTT
XM_017009971.2:c.10182+25_10182+26insTTTT	XP_016865460.1:n.10182+25_10182+26insTTTT
XM_017009972.1:c.3300+25_3300+26insTTTT	XP_016865461.1:n.3300+25_3300+26insTTTT
XM_017009973.1:c.3279+25_3279+26insTTTT	XP_016865462.1:n.3279+25_3279+26insTTTT
XM_017009974.2:c.10182+25_10182+26insTTTT	XP_016865463.1:n.10182+25_10182+26insTTTT
XR_001742802.1:n.2523-9873_2523-9872insAAAA
NR_003149.2:n.10177+25_10177+26insTTTT