Canonical Allele Identifier: CA2767419660

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755208_90755209insAG , CM000667.2:g.90755208_90755209insAG	GRCh38
NC_000005.9:g.90051025_90051026insAG , CM000667.1:g.90051025_90051026insAG	GRCh37
NC_000005.8:g.90086781_90086782insAG	NCBI36
NG_007083.1:g.201409_201410insAG
NG_007083.2:g.230865_230866insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11580+23_11580+24insAG MANE Select	ENSP00000384582.2:n.11580+23_11580+24insAG
ENST00000425867.3:c.711+23_711+24insAG	ENSP00000392618.3:n.711+23_711+24insAG
ENST00000639431.1:c.265+78999_265+79000insAG	ENSP00000491057.1:n.265+78999_265+79000insAG
ENST00000640374.1:n.4724+23_4724+24insAG
ENST00000640464.1:n.1999+23_1999+24insAG
ENST00000405460.6:c.11580+23_11580+24insAG	ENSP00000384582.2:n.11580+23_11580+24insAG
ENST00000509621.1:c.4277+23_4277+24insAG
NM_032119.3:c.11580+23_11580+24insAG	NP_115495.3:n.11580+23_11580+24insAG
NR_003149.1:n.11593+23_11593+24insAG
XM_011543675.1:c.11577+23_11577+24insAG	XP_011541977.1:n.11577+23_11577+24insAG
XM_011543676.1:c.11499+23_11499+24insAG	XP_011541978.1:n.11499+23_11499+24insAG
XM_011543677.1:c.8883+23_8883+24insAG	XP_011541979.1:n.8883+23_8883+24insAG
XM_011543678.1:c.11580+23_11580+24insAG	XP_011541980.1:n.11580+23_11580+24insAG
NM_032119.4:c.11580+23_11580+24insAG MANE Select	NP_115495.3:n.11580+23_11580+24insAG
XM_017009963.2:c.11601+23_11601+24insAG	XP_016865452.1:n.11601+23_11601+24insAG
XM_017009964.2:c.11598+23_11598+24insAG	XP_016865453.1:n.11598+23_11598+24insAG
XM_017009965.1:c.11598+23_11598+24insAG	XP_016865454.1:n.11598+23_11598+24insAG
XM_017009966.2:c.11520+23_11520+24insAG	XP_016865455.1:n.11520+23_11520+24insAG
XM_017009967.1:c.11505+23_11505+24insAG	XP_016865456.1:n.11505+23_11505+24insAG
XM_017009968.2:c.11601+23_11601+24insAG	XP_016865457.1:n.11601+23_11601+24insAG
XM_017009969.2:c.11601+23_11601+24insAG	XP_016865458.1:n.11601+23_11601+24insAG
XM_017009970.2:c.11601+23_11601+24insAG	XP_016865459.1:n.11601+23_11601+24insAG
XM_017009971.2:c.11601+23_11601+24insAG	XP_016865460.1:n.11601+23_11601+24insAG
XM_017009972.1:c.4719+23_4719+24insAG	XP_016865461.1:n.4719+23_4719+24insAG
XM_017009973.1:c.4698+23_4698+24insAG	XP_016865462.1:n.4698+23_4698+24insAG
NR_003149.2:n.11596+23_11596+24insAG