Canonical Allele Identifier: CA3341206

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90774176T>C , CM000667.2:g.90774176T>C	GRCh38
NC_000005.9:g.90069993T>C , CM000667.1:g.90069993T>C	GRCh37
NC_000005.8:g.90105749T>C	NCBI36
NG_007083.1:g.220377T>C
NG_007083.2:g.249833T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12286-10T>C MANE Select	NP_115495.3:n.12286-10T>C
ENST00000405460.9:c.12286-10T>C MANE Select	ENSP00000384582.2:n.12286-10T>C
NM_032119.3:c.12286-10T>C	NP_115495.3:n.12286-10T>C
NR_003149.1:n.12299-10T>C
NR_003149.2:n.12302-10T>C
ENST00000405460.6:c.12286-10T>C	ENSP00000384582.2:n.12286-10T>C
ENST00000425867.3:c.1240-10T>C	ENSP00000392618.3:n.1240-10T>C
ENST00000639431.1:c.265+97967T>C	ENSP00000491057.1:n.265+97967T>C
ENST00000640464.1:n.2705-10T>C
ENST00000640729.1:n.863-10T>C
XM_011543675.1:c.12283-10T>C	XP_011541977.1:n.12283-10T>C
XM_011543676.1:c.12205-10T>C	XP_011541978.1:n.12205-10T>C
XM_011543677.1:c.9589-10T>C	XP_011541979.1:n.9589-10T>C
XM_011543678.1:c.12286-10T>C	XP_011541980.1:n.12286-10T>C
XM_017009963.2:c.12307-10T>C	XP_016865452.1:n.12307-10T>C
XM_017009964.2:c.12304-10T>C	XP_016865453.1:n.12304-10T>C
XM_017009965.1:c.12304-10T>C	XP_016865454.1:n.12304-10T>C
XM_017009966.2:c.12226-10T>C	XP_016865455.1:n.12226-10T>C
XM_017009967.1:c.12211-10T>C	XP_016865456.1:n.12211-10T>C
XM_017009968.2:c.12307-10T>C	XP_016865457.1:n.12307-10T>C
XM_017009969.2:c.12307-10T>C	XP_016865458.1:n.12307-10T>C
XM_017009970.2:c.12307-10T>C	XP_016865459.1:n.12307-10T>C
XM_017009971.2:c.12307-10T>C	XP_016865460.1:n.12307-10T>C
XM_017009972.1:c.5425-10T>C	XP_016865461.1:n.5425-10T>C
XM_017009973.1:c.5404-10T>C	XP_016865462.1:n.5404-10T>C