Canonical Allele Identifier: CA3341581

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90788064C>T , CM000667.2:g.90788064C>T	GRCh38
NC_000005.9:g.90083881C>T , CM000667.1:g.90083881C>T	GRCh37
NC_000005.8:g.90119637C>T	NCBI36
NG_007083.1:g.234265C>T
NG_007083.2:g.263721C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13654-7C>T MANE Select	NP_115495.3:n.13654-7C>T
ENST00000405460.9:c.13654-7C>T MANE Select	ENSP00000384582.2:n.13654-7C>T
NM_032119.3:c.13654-7C>T	NP_115495.3:n.13654-7C>T
NR_003149.1:n.13667-7C>T
NR_003149.2:n.13670-7C>T
ENST00000405460.6:c.13654-7C>T	ENSP00000384582.2:n.13654-7C>T
ENST00000425867.2:c.637-7C>T	ENSP00000392618.2:n.637-7C>T
ENST00000425867.3:c.2608-7C>T	ENSP00000392618.3:n.2608-7C>T
ENST00000638510.1:n.921-7C>T
ENST00000638975.1:c.283-7C>T	ENSP00000492630.1:n.283-7C>T
ENST00000639431.1:c.265+111855C>T	ENSP00000491057.1:n.265+111855C>T
ENST00000640407.1:c.64-7C>T	ENSP00000491425.1:n.64-7C>T
XM_011543675.1:c.13651-7C>T	XP_011541977.1:n.13651-7C>T
XM_011543676.1:c.13573-7C>T	XP_011541978.1:n.13573-7C>T
XM_011543677.1:c.10957-7C>T	XP_011541979.1:n.10957-7C>T
XM_011543678.1:c.13654-7C>T	XP_011541980.1:n.13654-7C>T
XM_017009963.2:c.13675-7C>T	XP_016865452.1:n.13675-7C>T
XM_017009964.2:c.13672-7C>T	XP_016865453.1:n.13672-7C>T
XM_017009965.1:c.13672-7C>T	XP_016865454.1:n.13672-7C>T
XM_017009966.2:c.13594-7C>T	XP_016865455.1:n.13594-7C>T
XM_017009967.1:c.13579-7C>T	XP_016865456.1:n.13579-7C>T
XM_017009968.2:c.13675-7C>T	XP_016865457.1:n.13675-7C>T
XM_017009969.2:c.13675-7C>T	XP_016865458.1:n.13675-7C>T
XM_017009970.2:c.13675-7C>T	XP_016865459.1:n.13675-7C>T
XM_017009971.2:c.13675-7C>T	XP_016865460.1:n.13675-7C>T
XM_017009972.1:c.6793-7C>T	XP_016865461.1:n.6793-7C>T
XM_017009973.1:c.6772-7C>T	XP_016865462.1:n.6772-7C>T