Canonical Allele Identifier: CA122815448

Gene: ADGRV1

Linked Data

• dbSNP Id: rs904150855
• MyVariant Identifiers: chr5:g.90040693A>C (hg19) ; chr5:g.90744876A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90744876A>C , CM000667.2:g.90744876A>C	GRCh38
NC_000005.9:g.90040693A>C , CM000667.1:g.90040693A>C	GRCh37
NC_000005.8:g.90076449A>C	NCBI36
NG_007083.1:g.191077A>C
NG_007083.2:g.220533A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10550-170A>C MANE Select	ENSP00000384582.2:n.10550-170A>C
ENST00000639431.1:c.265+68667A>C	ENSP00000491057.1:n.265+68667A>C
ENST00000640374.1:n.3694-170A>C
ENST00000640464.1:n.969-170A>C
ENST00000405460.6:c.10550-170A>C	ENSP00000384582.2:n.10550-170A>C
ENST00000509621.1:c.3247-170A>C
NM_032119.3:c.10550-170A>C	NP_115495.3:n.10550-170A>C
NR_003149.1:n.10563-170A>C
XM_011543675.1:c.10547-170A>C	XP_011541977.1:n.10547-170A>C
XM_011543676.1:c.10469-170A>C	XP_011541978.1:n.10469-170A>C
XM_011543677.1:c.7853-170A>C	XP_011541979.1:n.7853-170A>C
XM_011543678.1:c.10550-170A>C	XP_011541980.1:n.10550-170A>C
XM_011543679.1:c.10550-170A>C	XP_011541981.1:n.10550-170A>C
NM_032119.4:c.10550-170A>C MANE Select	NP_115495.3:n.10550-170A>C
XM_017009963.2:c.10571-170A>C	XP_016865452.1:n.10571-170A>C
XM_017009964.2:c.10568-170A>C	XP_016865453.1:n.10568-170A>C
XM_017009965.1:c.10568-170A>C	XP_016865454.1:n.10568-170A>C
XM_017009966.2:c.10490-170A>C	XP_016865455.1:n.10490-170A>C
XM_017009967.1:c.10475-170A>C	XP_016865456.1:n.10475-170A>C
XM_017009968.2:c.10571-170A>C	XP_016865457.1:n.10571-170A>C
XM_017009969.2:c.10571-170A>C	XP_016865458.1:n.10571-170A>C
XM_017009970.2:c.10571-170A>C	XP_016865459.1:n.10571-170A>C
XM_017009971.2:c.10571-170A>C	XP_016865460.1:n.10571-170A>C
XM_017009972.1:c.3689-170A>C	XP_016865461.1:n.3689-170A>C
XM_017009973.1:c.3668-170A>C	XP_016865462.1:n.3668-170A>C
XM_017009974.2:c.10571-170A>C	XP_016865463.1:n.10571-170A>C
NR_003149.2:n.10566-170A>C