Canonical Allele Identifier: CA3342597

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91072522C>T , CM000667.2:g.91072522C>T	GRCh38
NC_000005.9:g.90368339C>T , CM000667.1:g.90368339C>T	GRCh37
NC_000005.8:g.90404095C>T	NCBI36
NG_007083.1:g.518723C>T
NG_007083.2:g.548179C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18228C>T MANE Select	NP_115495.3:p.Phe6076=
ENST00000405460.9:c.18228C>T MANE Select	ENSP00000384582.2:p.Phe6076=
NM_032119.3:c.18228C>T	NP_115495.3:p.Phe6076=
NR_003149.1:n.18241C>T
NR_003149.2:n.18244C>T
ENST00000405460.6:c.18228C>T	ENSP00000384582.2:p.Phe6076=
ENST00000425867.2:c.5211C>T	ENSP00000392618.2:p.Phe1737=
ENST00000425867.3:c.7182C>T	ENSP00000392618.3:p.Phe2394=
ENST00000638510.1:n.5495C>T
ENST00000638990.1:c.1440C>T
ENST00000639431.1:c.520C>T	ENSP00000491057.1:n.520C>T
ENST00000639707.1:c.312C>T	ENSP00000492328.1:p.Phe104=
ENST00000639821.1:c.312C>T	ENSP00000492216.1:p.Phe104=
ENST00000640369.1:c.312C>T	ENSP00000491401.1:p.Phe104=
ENST00000640407.1:c.4677C>T	ENSP00000491425.1:n.4677C>T
ENST00000640815.1:c.312C>T	ENSP00000491767.1:p.Phe104=
XM_011543675.1:c.18225C>T	XP_011541977.1:p.Phe6075=
XM_011543676.1:c.18147C>T	XP_011541978.1:p.Phe6049=
XM_011543677.1:c.15531C>T	XP_011541979.1:p.Phe5177=
XM_017009963.2:c.18249C>T	XP_016865452.1:p.Phe6083=
XM_017009964.2:c.18246C>T	XP_016865453.1:p.Phe6082=
XM_017009965.1:c.18246C>T	XP_016865454.1:p.Phe6082=
XM_017009966.2:c.18168C>T	XP_016865455.1:p.Phe6056=
XM_017009967.1:c.18153C>T	XP_016865456.1:p.Phe6051=
XM_017009968.2:c.18069C>T	XP_016865457.1:p.Phe6023=
XM_017009969.2:c.18249C>T	XP_016865458.1:p.Phe6083=
XM_017009972.1:c.11367C>T	XP_016865461.1:p.Phe3789=
XM_017009973.1:c.11346C>T	XP_016865462.1:p.Phe3782=