Canonical Allele Identifier: CA360403210

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021389A>C (hg19) ; chr5:g.90725572A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725572A>C , CM000667.2:g.90725572A>C	GRCh38
NC_000005.9:g.90021389A>C , CM000667.1:g.90021389A>C	GRCh37
NC_000005.8:g.90057145A>C	NCBI36
NG_007083.1:g.171773A>C
NG_007083.2:g.201229A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10077A>C MANE Select	ENSP00000384582.2:p.Glu3359Asp
ENST00000639431.1:c.265+49363A>C	ENSP00000491057.1:n.265+49363A>C
ENST00000640374.1:n.3221A>C
ENST00000640464.1:n.496A>C
ENST00000405460.6:c.10077A>C	ENSP00000384582.2:p.Glu3359Asp
ENST00000509621.1:c.2774A>C
NM_032119.3:c.10077A>C	NP_115495.3:p.Glu3359Asp
NR_003149.1:n.10090A>C
XM_011543675.1:c.10074A>C	XP_011541977.1:p.Glu3358Asp
XM_011543676.1:c.9996A>C	XP_011541978.1:p.Glu3332Asp
XM_011543677.1:c.7380A>C	XP_011541979.1:p.Glu2460Asp
XM_011543678.1:c.10077A>C	XP_011541980.1:p.Glu3359Asp
XM_011543679.1:c.10077A>C	XP_011541981.1:p.Glu3359Asp
XR_948560.1:n.272-9763T>G
NM_032119.4:c.10077A>C MANE Select	NP_115495.3:p.Glu3359Asp
XM_017009963.2:c.10098A>C	XP_016865452.1:p.Glu3366Asp
XM_017009964.2:c.10095A>C	XP_016865453.1:p.Glu3365Asp
XM_017009965.1:c.10095A>C	XP_016865454.1:p.Glu3365Asp
XM_017009966.2:c.10017A>C	XP_016865455.1:p.Glu3339Asp
XM_017009967.1:c.10002A>C	XP_016865456.1:p.Glu3334Asp
XM_017009968.2:c.10098A>C	XP_016865457.1:p.Glu3366Asp
XM_017009969.2:c.10098A>C	XP_016865458.1:p.Glu3366Asp
XM_017009970.2:c.10098A>C	XP_016865459.1:p.Glu3366Asp
XM_017009971.2:c.10098A>C	XP_016865460.1:p.Glu3366Asp
XM_017009972.1:c.3216A>C	XP_016865461.1:p.Glu1072Asp
XM_017009973.1:c.3195A>C	XP_016865462.1:p.Glu1065Asp
XM_017009974.2:c.10098A>C	XP_016865463.1:p.Glu3366Asp
XR_001742802.1:n.2523-9763T>G
NR_003149.2:n.10093A>C