Canonical Allele Identifier: CA445413777

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012462G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716645G>C , CM000667.2:g.90716645G>C	GRCh38
NC_000005.9:g.90012462G>C , CM000667.1:g.90012462G>C	GRCh37
NC_000005.8:g.90048218G>C	NCBI36
NG_007083.1:g.162846G>C
NG_007083.2:g.192302G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9363G>C MANE Select	ENSP00000384582.2:p.Val3121=
ENST00000639431.1:c.265+40436G>C	ENSP00000491057.1:n.265+40436G>C
ENST00000639473.1:n.4822G>C
ENST00000640012.1:c.3170G>C
ENST00000640374.1:n.2507G>C
ENST00000640779.1:c.4092G>C
ENST00000405460.6:c.9363G>C	ENSP00000384582.2:p.Val3121=
ENST00000509621.1:c.2060G>C
NM_032119.3:c.9363G>C	NP_115495.3:p.Val3121=
NR_003149.1:n.9376G>C
XM_011543675.1:c.9360G>C	XP_011541977.1:p.Val3120=
XM_011543676.1:c.9282G>C	XP_011541978.1:p.Val3094=
XM_011543677.1:c.6666G>C	XP_011541979.1:p.Val2222=
XM_011543678.1:c.9363G>C	XP_011541980.1:p.Val3121=
XM_011543679.1:c.9363G>C	XP_011541981.1:p.Val3121=
XR_948560.1:n.272-836C>G
NM_032119.4:c.9363G>C MANE Select	NP_115495.3:p.Val3121=
XM_017009963.2:c.9384G>C	XP_016865452.1:p.Val3128=
XM_017009964.2:c.9381G>C	XP_016865453.1:p.Val3127=
XM_017009965.1:c.9381G>C	XP_016865454.1:p.Val3127=
XM_017009966.2:c.9303G>C	XP_016865455.1:p.Val3101=
XM_017009967.1:c.9288G>C	XP_016865456.1:p.Val3096=
XM_017009968.2:c.9384G>C	XP_016865457.1:p.Val3128=
XM_017009969.2:c.9384G>C	XP_016865458.1:p.Val3128=
XM_017009970.2:c.9384G>C	XP_016865459.1:p.Val3128=
XM_017009971.2:c.9384G>C	XP_016865460.1:p.Val3128=
XM_017009972.1:c.2502G>C	XP_016865461.1:p.Val834=
XM_017009973.1:c.2481G>C	XP_016865462.1:p.Val827=
XM_017009974.2:c.9384G>C	XP_016865463.1:p.Val3128=
XR_001742802.1:n.2523-836C>G
NR_003149.2:n.9379G>C