Canonical Allele Identifier: CA360403187

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021378A>T (hg19) ; chr5:g.90725561A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725561A>T , CM000667.2:g.90725561A>T	GRCh38
NC_000005.9:g.90021378A>T , CM000667.1:g.90021378A>T	GRCh37
NC_000005.8:g.90057134A>T	NCBI36
NG_007083.1:g.171762A>T
NG_007083.2:g.201218A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10066A>T MANE Select	ENSP00000384582.2:p.Ile3356Phe
ENST00000639431.1:c.265+49352A>T	ENSP00000491057.1:n.265+49352A>T
ENST00000640374.1:n.3210A>T
ENST00000640464.1:n.485A>T
ENST00000405460.6:c.10066A>T	ENSP00000384582.2:p.Ile3356Phe
ENST00000509621.1:c.2763A>T
NM_032119.3:c.10066A>T	NP_115495.3:p.Ile3356Phe
NR_003149.1:n.10079A>T
XM_011543675.1:c.10063A>T	XP_011541977.1:p.Ile3355Phe
XM_011543676.1:c.9985A>T	XP_011541978.1:p.Ile3329Phe
XM_011543677.1:c.7369A>T	XP_011541979.1:p.Ile2457Phe
XM_011543678.1:c.10066A>T	XP_011541980.1:p.Ile3356Phe
XM_011543679.1:c.10066A>T	XP_011541981.1:p.Ile3356Phe
XR_948560.1:n.272-9752T>A
NM_032119.4:c.10066A>T MANE Select	NP_115495.3:p.Ile3356Phe
XM_017009963.2:c.10087A>T	XP_016865452.1:p.Ile3363Phe
XM_017009964.2:c.10084A>T	XP_016865453.1:p.Ile3362Phe
XM_017009965.1:c.10084A>T	XP_016865454.1:p.Ile3362Phe
XM_017009966.2:c.10006A>T	XP_016865455.1:p.Ile3336Phe
XM_017009967.1:c.9991A>T	XP_016865456.1:p.Ile3331Phe
XM_017009968.2:c.10087A>T	XP_016865457.1:p.Ile3363Phe
XM_017009969.2:c.10087A>T	XP_016865458.1:p.Ile3363Phe
XM_017009970.2:c.10087A>T	XP_016865459.1:p.Ile3363Phe
XM_017009971.2:c.10087A>T	XP_016865460.1:p.Ile3363Phe
XM_017009972.1:c.3205A>T	XP_016865461.1:p.Ile1069Phe
XM_017009973.1:c.3184A>T	XP_016865462.1:p.Ile1062Phe
XM_017009974.2:c.10087A>T	XP_016865463.1:p.Ile3363Phe
XR_001742802.1:n.2523-9752T>A
NR_003149.2:n.10082A>T