Canonical Allele Identifier: CA360408996

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041463A>T (hg19) ; chr5:g.90745646A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745646A>T , CM000667.2:g.90745646A>T	GRCh38
NC_000005.9:g.90041463A>T , CM000667.1:g.90041463A>T	GRCh37
NC_000005.8:g.90077219A>T	NCBI36
NG_007083.1:g.191847A>T
NG_007083.2:g.221303A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10825A>T MANE Select	ENSP00000384582.2:p.Ile3609Phe
ENST00000639431.1:c.265+69437A>T	ENSP00000491057.1:n.265+69437A>T
ENST00000640374.1:n.3969A>T
ENST00000640464.1:n.1244A>T
ENST00000405460.6:c.10825A>T	ENSP00000384582.2:p.Ile3609Phe
ENST00000509621.1:c.3522A>T
NM_032119.3:c.10825A>T	NP_115495.3:p.Ile3609Phe
NR_003149.1:n.10838A>T
XM_011543675.1:c.10822A>T	XP_011541977.1:p.Ile3608Phe
XM_011543676.1:c.10744A>T	XP_011541978.1:p.Ile3582Phe
XM_011543677.1:c.8128A>T	XP_011541979.1:p.Ile2710Phe
XM_011543678.1:c.10825A>T	XP_011541980.1:p.Ile3609Phe
XM_011543679.1:c.*47A>T	XP_011541981.1:n.*47A>T
NM_032119.4:c.10825A>T MANE Select	NP_115495.3:p.Ile3609Phe
XM_017009963.2:c.10846A>T	XP_016865452.1:p.Ile3616Phe
XM_017009964.2:c.10843A>T	XP_016865453.1:p.Ile3615Phe
XM_017009965.1:c.10843A>T	XP_016865454.1:p.Ile3615Phe
XM_017009966.2:c.10765A>T	XP_016865455.1:p.Ile3589Phe
XM_017009967.1:c.10750A>T	XP_016865456.1:p.Ile3584Phe
XM_017009968.2:c.10846A>T	XP_016865457.1:p.Ile3616Phe
XM_017009969.2:c.10846A>T	XP_016865458.1:p.Ile3616Phe
XM_017009970.2:c.10846A>T	XP_016865459.1:p.Ile3616Phe
XM_017009971.2:c.10846A>T	XP_016865460.1:p.Ile3616Phe
XM_017009972.1:c.3964A>T	XP_016865461.1:p.Ile1322Phe
XM_017009973.1:c.3943A>T	XP_016865462.1:p.Ile1315Phe
XM_017009974.2:c.*47A>T	XP_016865463.1:n.*47A>T
NR_003149.2:n.10841A>T