Canonical Allele Identifier: CA360397625

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012487T>C (hg19) ; chr5:g.90716670T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716670T>C , CM000667.2:g.90716670T>C	GRCh38
NC_000005.9:g.90012487T>C , CM000667.1:g.90012487T>C	GRCh37
NC_000005.8:g.90048243T>C	NCBI36
NG_007083.1:g.162871T>C
NG_007083.2:g.192327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9388T>C MANE Select	ENSP00000384582.2:p.Ser3130Pro
ENST00000639431.1:c.265+40461T>C	ENSP00000491057.1:n.265+40461T>C
ENST00000639473.1:n.4847T>C
ENST00000640012.1:c.3195T>C
ENST00000640374.1:n.2532T>C
ENST00000640779.1:c.4117T>C
ENST00000405460.6:c.9388T>C	ENSP00000384582.2:p.Ser3130Pro
ENST00000509621.1:c.2085T>C
NM_032119.3:c.9388T>C	NP_115495.3:p.Ser3130Pro
NR_003149.1:n.9401T>C
XM_011543675.1:c.9385T>C	XP_011541977.1:p.Ser3129Pro
XM_011543676.1:c.9307T>C	XP_011541978.1:p.Ser3103Pro
XM_011543677.1:c.6691T>C	XP_011541979.1:p.Ser2231Pro
XM_011543678.1:c.9388T>C	XP_011541980.1:p.Ser3130Pro
XM_011543679.1:c.9388T>C	XP_011541981.1:p.Ser3130Pro
XR_948560.1:n.272-861A>G
NM_032119.4:c.9388T>C MANE Select	NP_115495.3:p.Ser3130Pro
XM_017009963.2:c.9409T>C	XP_016865452.1:p.Ser3137Pro
XM_017009964.2:c.9406T>C	XP_016865453.1:p.Ser3136Pro
XM_017009965.1:c.9406T>C	XP_016865454.1:p.Ser3136Pro
XM_017009966.2:c.9328T>C	XP_016865455.1:p.Ser3110Pro
XM_017009967.1:c.9313T>C	XP_016865456.1:p.Ser3105Pro
XM_017009968.2:c.9409T>C	XP_016865457.1:p.Ser3137Pro
XM_017009969.2:c.9409T>C	XP_016865458.1:p.Ser3137Pro
XM_017009970.2:c.9409T>C	XP_016865459.1:p.Ser3137Pro
XM_017009971.2:c.9409T>C	XP_016865460.1:p.Ser3137Pro
XM_017009972.1:c.2527T>C	XP_016865461.1:p.Ser843Pro
XM_017009973.1:c.2506T>C	XP_016865462.1:p.Ser836Pro
XM_017009974.2:c.9409T>C	XP_016865463.1:p.Ser3137Pro
XR_001742802.1:n.2523-861A>G
NR_003149.2:n.9404T>C