Canonical Allele Identifier: CA360409785

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745793C>T , CM000667.2:g.90745793C>T	GRCh38
NC_000005.9:g.90041610C>T , CM000667.1:g.90041610C>T	GRCh37
NC_000005.8:g.90077366C>T	NCBI36
NG_007083.1:g.191994C>T
NG_007083.2:g.221450C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10972C>T MANE Select	NP_115495.3:p.Gln3658Ter
ENST00000405460.9:c.10972C>T MANE Select	ENSP00000384582.2:p.Gln3658Ter
NM_032119.3:c.10972C>T	NP_115495.3:p.Gln3658Ter
NR_003149.1:n.10985C>T
NR_003149.2:n.10988C>T
ENST00000405460.6:c.10972C>T	ENSP00000384582.2:p.Gln3658Ter
ENST00000425867.3:c.103C>T	ENSP00000392618.3:p.Gln35Ter
ENST00000509621.1:c.3669C>T
ENST00000639431.1:c.265+69584C>T	ENSP00000491057.1:n.265+69584C>T
ENST00000640374.1:n.4116C>T
ENST00000640464.1:n.1391C>T
XM_011543675.1:c.10969C>T	XP_011541977.1:p.Gln3657Ter
XM_011543676.1:c.10891C>T	XP_011541978.1:p.Gln3631Ter
XM_011543677.1:c.8275C>T	XP_011541979.1:p.Gln2759Ter
XM_011543678.1:c.10972C>T	XP_011541980.1:p.Gln3658Ter
XM_017009963.2:c.10993C>T	XP_016865452.1:p.Gln3665Ter
XM_017009964.2:c.10990C>T	XP_016865453.1:p.Gln3664Ter
XM_017009965.1:c.10990C>T	XP_016865454.1:p.Gln3664Ter
XM_017009966.2:c.10912C>T	XP_016865455.1:p.Gln3638Ter
XM_017009967.1:c.10897C>T	XP_016865456.1:p.Gln3633Ter
XM_017009968.2:c.10993C>T	XP_016865457.1:p.Gln3665Ter
XM_017009969.2:c.10993C>T	XP_016865458.1:p.Gln3665Ter
XM_017009970.2:c.10993C>T	XP_016865459.1:p.Gln3665Ter
XM_017009971.2:c.10993C>T	XP_016865460.1:p.Gln3665Ter
XM_017009972.1:c.4111C>T	XP_016865461.1:p.Gln1371Ter
XM_017009973.1:c.4090C>T	XP_016865462.1:p.Gln1364Ter