Canonical Allele Identifier: CA360409484

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041557T>C (hg19) ; chr5:g.90745740T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745740T>C , CM000667.2:g.90745740T>C	GRCh38
NC_000005.9:g.90041557T>C , CM000667.1:g.90041557T>C	GRCh37
NC_000005.8:g.90077313T>C	NCBI36
NG_007083.1:g.191941T>C
NG_007083.2:g.221397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10919T>C MANE Select	ENSP00000384582.2:p.Val3640Ala
ENST00000425867.3:c.50T>C	ENSP00000392618.3:p.Val17Ala
ENST00000639431.1:c.265+69531T>C	ENSP00000491057.1:n.265+69531T>C
ENST00000640374.1:n.4063T>C
ENST00000640464.1:n.1338T>C
ENST00000405460.6:c.10919T>C	ENSP00000384582.2:p.Val3640Ala
ENST00000509621.1:c.3616T>C
NM_032119.3:c.10919T>C	NP_115495.3:p.Val3640Ala
NR_003149.1:n.10932T>C
XM_011543675.1:c.10916T>C	XP_011541977.1:p.Val3639Ala
XM_011543676.1:c.10838T>C	XP_011541978.1:p.Val3613Ala
XM_011543677.1:c.8222T>C	XP_011541979.1:p.Val2741Ala
XM_011543678.1:c.10919T>C	XP_011541980.1:p.Val3640Ala
NM_032119.4:c.10919T>C MANE Select	NP_115495.3:p.Val3640Ala
XM_017009963.2:c.10940T>C	XP_016865452.1:p.Val3647Ala
XM_017009964.2:c.10937T>C	XP_016865453.1:p.Val3646Ala
XM_017009965.1:c.10937T>C	XP_016865454.1:p.Val3646Ala
XM_017009966.2:c.10859T>C	XP_016865455.1:p.Val3620Ala
XM_017009967.1:c.10844T>C	XP_016865456.1:p.Val3615Ala
XM_017009968.2:c.10940T>C	XP_016865457.1:p.Val3647Ala
XM_017009969.2:c.10940T>C	XP_016865458.1:p.Val3647Ala
XM_017009970.2:c.10940T>C	XP_016865459.1:p.Val3647Ala
XM_017009971.2:c.10940T>C	XP_016865460.1:p.Val3647Ala
XM_017009972.1:c.4058T>C	XP_016865461.1:p.Val1353Ala
XM_017009973.1:c.4037T>C	XP_016865462.1:p.Val1346Ala
NR_003149.2:n.10935T>C