Canonical Allele Identifier: CA360390776

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89940593C>G (hg19) ; chr5:g.90644776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644776C>G , CM000667.2:g.90644776C>G	GRCh38
NC_000005.9:g.89940593C>G , CM000667.1:g.89940593C>G	GRCh37
NC_000005.8:g.89976349C>G	NCBI36
NG_007083.1:g.90977C>G
NG_007083.2:g.120433C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2805C>G MANE Select	ENSP00000384582.2:p.Asp935Glu
ENST00000504142.2:n.1571C>G
ENST00000639676.1:n.403C>G
ENST00000640403.1:c.108C>G	ENSP00000492531.1:p.Asp36Glu
ENST00000405460.6:c.2805C>G	ENSP00000384582.2:p.Asp935Glu
ENST00000504142.1:c.1570C>G
NM_032119.3:c.2805C>G	NP_115495.3:p.Asp935Glu
NR_003149.1:n.2901C>G
XM_011543675.1:c.2805C>G	XP_011541977.1:p.Asp935Glu
XM_011543676.1:c.2805C>G	XP_011541978.1:p.Asp935Glu
XM_011543677.1:c.108C>G	XP_011541979.1:p.Asp36Glu
XM_011543678.1:c.2805C>G	XP_011541980.1:p.Asp935Glu
XM_011543679.1:c.2805C>G	XP_011541981.1:p.Asp935Glu
NM_032119.4:c.2805C>G MANE Select	NP_115495.3:p.Asp935Glu
XM_017009963.2:c.2805C>G	XP_016865452.1:p.Asp935Glu
XM_017009964.2:c.2805C>G	XP_016865453.1:p.Asp935Glu
XM_017009965.1:c.2802C>G	XP_016865454.1:p.Asp934Glu
XM_017009966.2:c.2805C>G	XP_016865455.1:p.Asp935Glu
XM_017009967.1:c.2709C>G	XP_016865456.1:p.Asp903Glu
XM_017009968.2:c.2805C>G	XP_016865457.1:p.Asp935Glu
XM_017009969.2:c.2805C>G	XP_016865458.1:p.Asp935Glu
XM_017009970.2:c.2805C>G	XP_016865459.1:p.Asp935Glu
XM_017009971.2:c.2805C>G	XP_016865460.1:p.Asp935Glu
XM_017009974.2:c.2805C>G	XP_016865463.1:p.Asp935Glu
NR_003149.2:n.2904C>G