Canonical Allele Identifier: CA445413670

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012429A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716612A>C , CM000667.2:g.90716612A>C	GRCh38
NC_000005.9:g.90012429A>C , CM000667.1:g.90012429A>C	GRCh37
NC_000005.8:g.90048185A>C	NCBI36
NG_007083.1:g.162813A>C
NG_007083.2:g.192269A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9330A>C MANE Select	ENSP00000384582.2:p.Gly3110=
ENST00000639431.1:c.265+40403A>C	ENSP00000491057.1:n.265+40403A>C
ENST00000639473.1:n.4789A>C
ENST00000640012.1:c.3137A>C
ENST00000640374.1:n.2474A>C
ENST00000640779.1:c.4059A>C
ENST00000405460.6:c.9330A>C	ENSP00000384582.2:p.Gly3110=
ENST00000509621.1:c.2027A>C
NM_032119.3:c.9330A>C	NP_115495.3:p.Gly3110=
NR_003149.1:n.9343A>C
XM_011543675.1:c.9327A>C	XP_011541977.1:p.Gly3109=
XM_011543676.1:c.9249A>C	XP_011541978.1:p.Gly3083=
XM_011543677.1:c.6633A>C	XP_011541979.1:p.Gly2211=
XM_011543678.1:c.9330A>C	XP_011541980.1:p.Gly3110=
XM_011543679.1:c.9330A>C	XP_011541981.1:p.Gly3110=
XR_948560.1:n.272-803T>G
NM_032119.4:c.9330A>C MANE Select	NP_115495.3:p.Gly3110=
XM_017009963.2:c.9351A>C	XP_016865452.1:p.Gly3117=
XM_017009964.2:c.9348A>C	XP_016865453.1:p.Gly3116=
XM_017009965.1:c.9348A>C	XP_016865454.1:p.Gly3116=
XM_017009966.2:c.9270A>C	XP_016865455.1:p.Gly3090=
XM_017009967.1:c.9255A>C	XP_016865456.1:p.Gly3085=
XM_017009968.2:c.9351A>C	XP_016865457.1:p.Gly3117=
XM_017009969.2:c.9351A>C	XP_016865458.1:p.Gly3117=
XM_017009970.2:c.9351A>C	XP_016865459.1:p.Gly3117=
XM_017009971.2:c.9351A>C	XP_016865460.1:p.Gly3117=
XM_017009972.1:c.2469A>C	XP_016865461.1:p.Gly823=
XM_017009973.1:c.2448A>C	XP_016865462.1:p.Gly816=
XM_017009974.2:c.9351A>C	XP_016865463.1:p.Gly3117=
XR_001742802.1:n.2523-803T>G
NR_003149.2:n.9346A>C