Canonical Allele Identifier: CA1562956692

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90913821_90913822delinsAT , CM000667.2:g.90913821_90913822delinsAT	GRCh38
NC_000005.9:g.90209638_90209639delinsAT , CM000667.1:g.90209638_90209639delinsAT	GRCh37
NC_000005.8:g.90245394_90245395delinsAT	NCBI36
NG_007083.1:g.360022_360023delinsAT
NG_007083.2:g.389478_389479delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.17856+49964_17856+49965delinsAT MANE Select	ENSP00000384582.2:n.17856+49964_17856+49965delinsAT
ENST00000425867.3:c.6810+49964_6810+49965delinsAT	ENSP00000392618.3:n.6810+49964_6810+49965delinsAT
ENST00000638510.1:n.5123+49964_5123+49965delinsAT
ENST00000638990.1:c.1068+49964_1068+49965delinsAT
ENST00000639431.1:c.266-71523_266-71522delinsAT	ENSP00000491057.1:n.266-71523_266-71522delinsAT
ENST00000640407.1:c.4305+49964_4305+49965delinsAT	ENSP00000491425.1:n.4305+49964_4305+49965delinsAT
ENST00000640815.1:c.-61+14498_-61+14499delinsAT	ENSP00000491767.1:n.-61+14498_-61+14499delinsAT
ENST00000405460.6:c.17856+49964_17856+49965delinsAT	ENSP00000384582.2:n.17856+49964_17856+49965delinsAT
ENST00000425867.2:c.4839+49964_4839+49965delinsAT	ENSP00000392618.2:n.4839+49964_4839+49965delinsAT
NM_032119.3:c.17856+49964_17856+49965delinsAT	NP_115495.3:n.17856+49964_17856+49965delinsAT
NR_003149.1:n.17869+49964_17869+49965delinsAT
XM_011543675.1:c.17853+49964_17853+49965delinsAT	XP_011541977.1:n.17853+49964_17853+49965delinsAT
XM_011543676.1:c.17775+49964_17775+49965delinsAT	XP_011541978.1:n.17775+49964_17775+49965delinsAT
XM_011543677.1:c.15159+49964_15159+49965delinsAT	XP_011541979.1:n.15159+49964_15159+49965delinsAT
NM_032119.4:c.17856+49964_17856+49965delinsAT MANE Select	NP_115495.3:n.17856+49964_17856+49965delinsAT
XM_017009963.2:c.17877+49964_17877+49965delinsAT	XP_016865452.1:n.17877+49964_17877+49965delinsAT
XM_017009964.2:c.17874+49964_17874+49965delinsAT	XP_016865453.1:n.17874+49964_17874+49965delinsAT
XM_017009965.1:c.17874+49964_17874+49965delinsAT	XP_016865454.1:n.17874+49964_17874+49965delinsAT
XM_017009966.2:c.17796+49964_17796+49965delinsAT	XP_016865455.1:n.17796+49964_17796+49965delinsAT
XM_017009967.1:c.17781+49964_17781+49965delinsAT	XP_016865456.1:n.17781+49964_17781+49965delinsAT
XM_017009968.2:c.17697+49964_17697+49965delinsAT	XP_016865457.1:n.17697+49964_17697+49965delinsAT
XM_017009969.2:c.17877+49964_17877+49965delinsAT	XP_016865458.1:n.17877+49964_17877+49965delinsAT
XM_017009972.1:c.10995+49964_10995+49965delinsAT	XP_016865461.1:n.10995+49964_10995+49965delinsAT
XM_017009973.1:c.10974+49964_10974+49965delinsAT	XP_016865462.1:n.10974+49964_10974+49965delinsAT
NR_003149.2:n.17872+49964_17872+49965delinsAT