Canonical Allele Identifier: CA360409041

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041473A>T (hg19) ; chr5:g.90745656A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745656A>T , CM000667.2:g.90745656A>T	GRCh38
NC_000005.9:g.90041473A>T , CM000667.1:g.90041473A>T	GRCh37
NC_000005.8:g.90077229A>T	NCBI36
NG_007083.1:g.191857A>T
NG_007083.2:g.221313A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10835A>T MANE Select	ENSP00000384582.2:p.Asp3612Val
ENST00000639431.1:c.265+69447A>T	ENSP00000491057.1:n.265+69447A>T
ENST00000640374.1:n.3979A>T
ENST00000640464.1:n.1254A>T
ENST00000405460.6:c.10835A>T	ENSP00000384582.2:p.Asp3612Val
ENST00000509621.1:c.3532A>T
NM_032119.3:c.10835A>T	NP_115495.3:p.Asp3612Val
NR_003149.1:n.10848A>T
XM_011543675.1:c.10832A>T	XP_011541977.1:p.Asp3611Val
XM_011543676.1:c.10754A>T	XP_011541978.1:p.Asp3585Val
XM_011543677.1:c.8138A>T	XP_011541979.1:p.Asp2713Val
XM_011543678.1:c.10835A>T	XP_011541980.1:p.Asp3612Val
XM_011543679.1:c.*57A>T	XP_011541981.1:n.*57A>T
NM_032119.4:c.10835A>T MANE Select	NP_115495.3:p.Asp3612Val
XM_017009963.2:c.10856A>T	XP_016865452.1:p.Asp3619Val
XM_017009964.2:c.10853A>T	XP_016865453.1:p.Asp3618Val
XM_017009965.1:c.10853A>T	XP_016865454.1:p.Asp3618Val
XM_017009966.2:c.10775A>T	XP_016865455.1:p.Asp3592Val
XM_017009967.1:c.10760A>T	XP_016865456.1:p.Asp3587Val
XM_017009968.2:c.10856A>T	XP_016865457.1:p.Asp3619Val
XM_017009969.2:c.10856A>T	XP_016865458.1:p.Asp3619Val
XM_017009970.2:c.10856A>T	XP_016865459.1:p.Asp3619Val
XM_017009971.2:c.10856A>T	XP_016865460.1:p.Asp3619Val
XM_017009972.1:c.3974A>T	XP_016865461.1:p.Asp1325Val
XM_017009973.1:c.3953A>T	XP_016865462.1:p.Asp1318Val
XM_017009974.2:c.*57A>T	XP_016865463.1:n.*57A>T
NR_003149.2:n.10851A>T