Canonical Allele Identifier: CA360397649

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012493G>C (hg19) ; chr5:g.90716676G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716676G>C , CM000667.2:g.90716676G>C	GRCh38
NC_000005.9:g.90012493G>C , CM000667.1:g.90012493G>C	GRCh37
NC_000005.8:g.90048249G>C	NCBI36
NG_007083.1:g.162877G>C
NG_007083.2:g.192333G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9394G>C MANE Select	ENSP00000384582.2:p.Asp3132His
ENST00000639431.1:c.265+40467G>C	ENSP00000491057.1:n.265+40467G>C
ENST00000639473.1:n.4853G>C
ENST00000640012.1:c.3201G>C
ENST00000640374.1:n.2538G>C
ENST00000640779.1:c.4123G>C
ENST00000405460.6:c.9394G>C	ENSP00000384582.2:p.Asp3132His
ENST00000509621.1:c.2091G>C
NM_032119.3:c.9394G>C	NP_115495.3:p.Asp3132His
NR_003149.1:n.9407G>C
XM_011543675.1:c.9391G>C	XP_011541977.1:p.Asp3131His
XM_011543676.1:c.9313G>C	XP_011541978.1:p.Asp3105His
XM_011543677.1:c.6697G>C	XP_011541979.1:p.Asp2233His
XM_011543678.1:c.9394G>C	XP_011541980.1:p.Asp3132His
XM_011543679.1:c.9394G>C	XP_011541981.1:p.Asp3132His
XR_948560.1:n.272-867C>G
NM_032119.4:c.9394G>C MANE Select	NP_115495.3:p.Asp3132His
XM_017009963.2:c.9415G>C	XP_016865452.1:p.Asp3139His
XM_017009964.2:c.9412G>C	XP_016865453.1:p.Asp3138His
XM_017009965.1:c.9412G>C	XP_016865454.1:p.Asp3138His
XM_017009966.2:c.9334G>C	XP_016865455.1:p.Asp3112His
XM_017009967.1:c.9319G>C	XP_016865456.1:p.Asp3107His
XM_017009968.2:c.9415G>C	XP_016865457.1:p.Asp3139His
XM_017009969.2:c.9415G>C	XP_016865458.1:p.Asp3139His
XM_017009970.2:c.9415G>C	XP_016865459.1:p.Asp3139His
XM_017009971.2:c.9415G>C	XP_016865460.1:p.Asp3139His
XM_017009972.1:c.2533G>C	XP_016865461.1:p.Asp845His
XM_017009973.1:c.2512G>C	XP_016865462.1:p.Asp838His
XM_017009974.2:c.9415G>C	XP_016865463.1:p.Asp3139His
XR_001742802.1:n.2523-867C>G
NR_003149.2:n.9410G>C