Canonical Allele Identifier: CA360367139

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050955A>G (hg19) ; chr5:g.90755138A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755138A>G , CM000667.2:g.90755138A>G	GRCh38
NC_000005.9:g.90050955A>G , CM000667.1:g.90050955A>G	GRCh37
NC_000005.8:g.90086711A>G	NCBI36
NG_007083.1:g.201339A>G
NG_007083.2:g.230795A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11533A>G MANE Select	ENSP00000384582.2:p.Met3845Val
ENST00000425867.3:c.664A>G	ENSP00000392618.3:p.Met222Val
ENST00000639431.1:c.265+78929A>G	ENSP00000491057.1:n.265+78929A>G
ENST00000640374.1:n.4677A>G
ENST00000640464.1:n.1952A>G
ENST00000405460.6:c.11533A>G	ENSP00000384582.2:p.Met3845Val
ENST00000509621.1:c.4230A>G
NM_032119.3:c.11533A>G	NP_115495.3:p.Met3845Val
NR_003149.1:n.11546A>G
XM_011543675.1:c.11530A>G	XP_011541977.1:p.Met3844Val
XM_011543676.1:c.11452A>G	XP_011541978.1:p.Met3818Val
XM_011543677.1:c.8836A>G	XP_011541979.1:p.Met2946Val
XM_011543678.1:c.11533A>G	XP_011541980.1:p.Met3845Val
NM_032119.4:c.11533A>G MANE Select	NP_115495.3:p.Met3845Val
XM_017009963.2:c.11554A>G	XP_016865452.1:p.Met3852Val
XM_017009964.2:c.11551A>G	XP_016865453.1:p.Met3851Val
XM_017009965.1:c.11551A>G	XP_016865454.1:p.Met3851Val
XM_017009966.2:c.11473A>G	XP_016865455.1:p.Met3825Val
XM_017009967.1:c.11458A>G	XP_016865456.1:p.Met3820Val
XM_017009968.2:c.11554A>G	XP_016865457.1:p.Met3852Val
XM_017009969.2:c.11554A>G	XP_016865458.1:p.Met3852Val
XM_017009970.2:c.11554A>G	XP_016865459.1:p.Met3852Val
XM_017009971.2:c.11554A>G	XP_016865460.1:p.Met3852Val
XM_017009972.1:c.4672A>G	XP_016865461.1:p.Met1558Val
XM_017009973.1:c.4651A>G	XP_016865462.1:p.Met1551Val
NR_003149.2:n.11549A>G