Canonical Allele Identifier: CA360411242

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811149C>T , CM000667.2:g.90811149C>T	GRCh38
NC_000005.9:g.90106966C>T , CM000667.1:g.90106966C>T	GRCh37
NC_000005.8:g.90142722C>T	NCBI36
NG_007083.1:g.257350C>T
NG_007083.2:g.286806C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15889C>T MANE Select	NP_115495.3:p.Gln5297Ter
ENST00000405460.9:c.15889C>T MANE Select	ENSP00000384582.2:p.Gln5297Ter
NM_032119.3:c.15889C>T	NP_115495.3:p.Gln5297Ter
NR_003149.1:n.15902C>T
NR_003149.2:n.15905C>T
ENST00000405460.6:c.15889C>T	ENSP00000384582.2:p.Gln5297Ter
ENST00000425867.2:c.2872C>T	ENSP00000392618.2:p.Gln958Ter
ENST00000425867.3:c.4843C>T	ENSP00000392618.3:p.Gln1615Ter
ENST00000638510.1:n.3156C>T
ENST00000639431.1:c.265+134940C>T	ENSP00000491057.1:n.265+134940C>T
ENST00000640407.1:c.2299C>T	ENSP00000491425.1:p.Gln767Ter
XM_011543675.1:c.15886C>T	XP_011541977.1:p.Gln5296Ter
XM_011543676.1:c.15808C>T	XP_011541978.1:p.Gln5270Ter
XM_011543677.1:c.13192C>T	XP_011541979.1:p.Gln4398Ter
XM_017009963.2:c.15910C>T	XP_016865452.1:p.Gln5304Ter
XM_017009964.2:c.15907C>T	XP_016865453.1:p.Gln5303Ter
XM_017009965.1:c.15907C>T	XP_016865454.1:p.Gln5303Ter
XM_017009966.2:c.15829C>T	XP_016865455.1:p.Gln5277Ter
XM_017009967.1:c.15814C>T	XP_016865456.1:p.Gln5272Ter
XM_017009968.2:c.15730C>T	XP_016865457.1:p.Gln5244Ter
XM_017009969.2:c.15910C>T	XP_016865458.1:p.Gln5304Ter
XM_017009972.1:c.9028C>T	XP_016865461.1:p.Gln3010Ter
XM_017009973.1:c.9007C>T	XP_016865462.1:p.Gln3003Ter