Canonical Allele Identifier: CA3339831

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90689948T>C , CM000667.2:g.90689948T>C	GRCh38
NC_000005.9:g.89985765T>C , CM000667.1:g.89985765T>C	GRCh37
NC_000005.8:g.90021521T>C	NCBI36
NG_007083.1:g.136149T>C
NG_007083.2:g.165605T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6578T>C MANE Select	NP_115495.3:p.Ile2193Thr
ENST00000405460.9:c.6578T>C MANE Select	ENSP00000384582.2:p.Ile2193Thr
NM_032119.3:c.6578T>C	NP_115495.3:p.Ile2193Thr
NR_003149.1:n.6674T>C
NR_003149.2:n.6677T>C
ENST00000405460.6:c.6578T>C	ENSP00000384582.2:p.Ile2193Thr
ENST00000639431.1:c.265+13739T>C	ENSP00000491057.1:n.265+13739T>C
ENST00000639473.1:n.2037T>C
ENST00000640012.1:c.468T>C
ENST00000640403.1:c.3869T>C	ENSP00000492531.1:p.Ile1290Thr
ENST00000640779.1:c.1390T>C
XM_011543675.1:c.6575T>C	XP_011541977.1:p.Ile2192Thr
XM_011543676.1:c.6497T>C	XP_011541978.1:p.Ile2166Thr
XM_011543677.1:c.3881T>C	XP_011541979.1:p.Ile1294Thr
XM_011543678.1:c.6578T>C	XP_011541980.1:p.Ile2193Thr
XM_011543679.1:c.6578T>C	XP_011541981.1:p.Ile2193Thr
XM_017009963.2:c.6578T>C	XP_016865452.1:p.Ile2193Thr
XM_017009964.2:c.6575T>C	XP_016865453.1:p.Ile2192Thr
XM_017009965.1:c.6575T>C	XP_016865454.1:p.Ile2192Thr
XM_017009966.2:c.6497T>C	XP_016865455.1:p.Ile2166Thr
XM_017009967.1:c.6482T>C	XP_016865456.1:p.Ile2161Thr
XM_017009968.2:c.6578T>C	XP_016865457.1:p.Ile2193Thr
XM_017009969.2:c.6578T>C	XP_016865458.1:p.Ile2193Thr
XM_017009970.2:c.6578T>C	XP_016865459.1:p.Ile2193Thr
XM_017009971.2:c.6578T>C	XP_016865460.1:p.Ile2193Thr
XM_017009972.1:c.-222T>C	XP_016865461.1:n.-222T>C
XM_017009973.1:c.-222T>C	XP_016865462.1:n.-222T>C
XM_017009974.2:c.6578T>C	XP_016865463.1:p.Ile2193Thr