Canonical Allele Identifier: CA122798579

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1554104916

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755268_90755269insTCT , CM000667.2:g.90755268_90755269insTCT	GRCh38
NC_000005.9:g.90051085_90051086insTCT , CM000667.1:g.90051085_90051086insTCT	GRCh37
NC_000005.8:g.90086841_90086842insTCT	NCBI36
NG_007083.1:g.201469_201470insTCT
NG_007083.2:g.230925_230926insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11580+83_11580+84insTCT MANE Select	ENSP00000384582.2:n.11580+83_11580+84insTCT
ENST00000425867.3:c.711+83_711+84insTCT	ENSP00000392618.3:n.711+83_711+84insTCT
ENST00000639431.1:c.265+79059_265+79060insTCT	ENSP00000491057.1:n.265+79059_265+79060insTCT
ENST00000640374.1:n.4724+83_4724+84insTCT
ENST00000640464.1:n.1999+83_1999+84insTCT
ENST00000405460.6:c.11580+83_11580+84insTCT	ENSP00000384582.2:n.11580+83_11580+84insTCT
ENST00000509621.1:c.4277+83_4277+84insTCT
NM_032119.3:c.11580+83_11580+84insTCT	NP_115495.3:n.11580+83_11580+84insTCT
NR_003149.1:n.11593+83_11593+84insTCT
XM_011543675.1:c.11577+83_11577+84insTCT	XP_011541977.1:n.11577+83_11577+84insTCT
XM_011543676.1:c.11499+83_11499+84insTCT	XP_011541978.1:n.11499+83_11499+84insTCT
XM_011543677.1:c.8883+83_8883+84insTCT	XP_011541979.1:n.8883+83_8883+84insTCT
XM_011543678.1:c.11580+83_11580+84insTCT	XP_011541980.1:n.11580+83_11580+84insTCT
NM_032119.4:c.11580+83_11580+84insTCT MANE Select	NP_115495.3:n.11580+83_11580+84insTCT
XM_017009963.2:c.11601+83_11601+84insTCT	XP_016865452.1:n.11601+83_11601+84insTCT
XM_017009964.2:c.11598+83_11598+84insTCT	XP_016865453.1:n.11598+83_11598+84insTCT
XM_017009965.1:c.11598+83_11598+84insTCT	XP_016865454.1:n.11598+83_11598+84insTCT
XM_017009966.2:c.11520+83_11520+84insTCT	XP_016865455.1:n.11520+83_11520+84insTCT
XM_017009967.1:c.11505+83_11505+84insTCT	XP_016865456.1:n.11505+83_11505+84insTCT
XM_017009968.2:c.11601+83_11601+84insTCT	XP_016865457.1:n.11601+83_11601+84insTCT
XM_017009969.2:c.11601+83_11601+84insTCT	XP_016865458.1:n.11601+83_11601+84insTCT
XM_017009970.2:c.11601+83_11601+84insTCT	XP_016865459.1:n.11601+83_11601+84insTCT
XM_017009971.2:c.11601+83_11601+84insTCT	XP_016865460.1:n.11601+83_11601+84insTCT
XM_017009972.1:c.4719+83_4719+84insTCT	XP_016865461.1:n.4719+83_4719+84insTCT
XM_017009973.1:c.4698+83_4698+84insTCT	XP_016865462.1:n.4698+83_4698+84insTCT
NR_003149.2:n.11596+83_11596+84insTCT