Canonical Allele Identifier: CA360370451

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756632T>C , CM000667.2:g.90756632T>C	GRCh38
NC_000005.9:g.90052449T>C , CM000667.1:g.90052449T>C	GRCh37
NC_000005.8:g.90088205T>C	NCBI36
NG_007083.1:g.202833T>C
NG_007083.2:g.232289T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11757+2T>C MANE Select	NP_115495.3:n.11757+2T>C
ENST00000405460.9:c.11757+2T>C MANE Select	ENSP00000384582.2:n.11757+2T>C
NM_032119.3:c.11757+2T>C	NP_115495.3:n.11757+2T>C
NR_003149.1:n.11770+2T>C
NR_003149.2:n.11773+2T>C
ENST00000405460.6:c.11757+2T>C	ENSP00000384582.2:n.11757+2T>C
ENST00000425867.3:c.712-347T>C	ENSP00000392618.3:n.712-347T>C
ENST00000509621.1:c.4454+2T>C
ENST00000639431.1:c.265+80423T>C	ENSP00000491057.1:n.265+80423T>C
ENST00000639884.1:n.65T>C
ENST00000640374.1:n.4725-347T>C
ENST00000640464.1:n.2176+2T>C
XM_011543675.1:c.11754+2T>C	XP_011541977.1:n.11754+2T>C
XM_011543676.1:c.11676+2T>C	XP_011541978.1:n.11676+2T>C
XM_011543677.1:c.9060+2T>C	XP_011541979.1:n.9060+2T>C
XM_011543678.1:c.11757+2T>C	XP_011541980.1:n.11757+2T>C
XM_017009963.2:c.11778+2T>C	XP_016865452.1:n.11778+2T>C
XM_017009964.2:c.11775+2T>C	XP_016865453.1:n.11775+2T>C
XM_017009965.1:c.11775+2T>C	XP_016865454.1:n.11775+2T>C
XM_017009966.2:c.11697+2T>C	XP_016865455.1:n.11697+2T>C
XM_017009967.1:c.11682+2T>C	XP_016865456.1:n.11682+2T>C
XM_017009968.2:c.11778+2T>C	XP_016865457.1:n.11778+2T>C
XM_017009969.2:c.11778+2T>C	XP_016865458.1:n.11778+2T>C
XM_017009970.2:c.11778+2T>C	XP_016865459.1:n.11778+2T>C
XM_017009971.2:c.11778+2T>C	XP_016865460.1:n.11778+2T>C
XM_017009972.1:c.4896+2T>C	XP_016865461.1:n.4896+2T>C
XM_017009973.1:c.4875+2T>C	XP_016865462.1:n.4875+2T>C