Canonical Allele Identifier: CA122797324

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90693958T>C , CM000667.2:g.90693958T>C	GRCh38
NC_000005.9:g.89989775T>C , CM000667.1:g.89989775T>C	GRCh37
NC_000005.8:g.90025531T>C	NCBI36
NG_007083.1:g.140159T>C
NG_007083.2:g.169615T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.7202T>C MANE Select	NP_115495.3:p.Met2401Thr
ENST00000405460.9:c.7202T>C MANE Select	ENSP00000384582.2:p.Met2401Thr
NM_032119.3:c.7202T>C	NP_115495.3:p.Met2401Thr
NR_003149.1:n.7215T>C
NR_003149.2:n.7218T>C
ENST00000405460.6:c.7202T>C	ENSP00000384582.2:p.Met2401Thr
ENST00000639431.1:c.265+17749T>C	ENSP00000491057.1:n.265+17749T>C
ENST00000639473.1:n.2661T>C
ENST00000640012.1:c.1009T>C
ENST00000640374.1:n.346T>C
ENST00000640403.1:c.4493T>C	ENSP00000492531.1:p.Met1498Thr
ENST00000640779.1:c.1931T>C
XM_011543675.1:c.7199T>C	XP_011541977.1:p.Met2400Thr
XM_011543676.1:c.7121T>C	XP_011541978.1:p.Met2374Thr
XM_011543677.1:c.4505T>C	XP_011541979.1:p.Met1502Thr
XM_011543678.1:c.7202T>C	XP_011541980.1:p.Met2401Thr
XM_011543679.1:c.7202T>C	XP_011541981.1:p.Met2401Thr
XM_017009963.2:c.7202T>C	XP_016865452.1:p.Met2401Thr
XM_017009964.2:c.7199T>C	XP_016865453.1:p.Met2400Thr
XM_017009965.1:c.7199T>C	XP_016865454.1:p.Met2400Thr
XM_017009966.2:c.7121T>C	XP_016865455.1:p.Met2374Thr
XM_017009967.1:c.7106T>C	XP_016865456.1:p.Met2369Thr
XM_017009968.2:c.7202T>C	XP_016865457.1:p.Met2401Thr
XM_017009969.2:c.7202T>C	XP_016865458.1:p.Met2401Thr
XM_017009970.2:c.7202T>C	XP_016865459.1:p.Met2401Thr
XM_017009971.2:c.7202T>C	XP_016865460.1:p.Met2401Thr
XM_017009972.1:c.320T>C	XP_016865461.1:p.Met107Thr
XM_017009973.1:c.320T>C	XP_016865462.1:p.Met107Thr
XM_017009974.2:c.7202T>C	XP_016865463.1:p.Met2401Thr