Canonical Allele Identifier: CA1562918271

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823494T= , CM000667.2:g.90823494T=	GRCh38
NC_000005.9:g.90119311T= , CM000667.1:g.90119311T=	GRCh37
NC_000005.8:g.90155067T=	NCBI36
NG_007083.1:g.269695T=
NG_007083.2:g.299151T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16266T= MANE Select	ENSP00000384582.2:p.Asp5422=
ENST00000425867.3:c.5220T=	ENSP00000392618.3:p.Asp1740=
ENST00000638510.1:n.3533T=
ENST00000639431.1:c.265+147285T=	ENSP00000491057.1:n.265+147285T=
ENST00000640061.1:n.128+1312T=
ENST00000640407.1:c.2676T=	ENSP00000491425.1:p.Asp892=
ENST00000405460.6:c.16266T=	ENSP00000384582.2:p.Asp5422=
ENST00000425867.2:c.3249T=	ENSP00000392618.2:p.Asp1083=
NM_032119.3:c.16266T=	NP_115495.3:p.Asp5422=
NR_003149.1:n.16279T=
XM_011543675.1:c.16263T=	XP_011541977.1:p.Asp5421=
XM_011543676.1:c.16185T=	XP_011541978.1:p.Asp5395=
XM_011543677.1:c.13569T=	XP_011541979.1:p.Asp4523=
NM_032119.4:c.16266T= MANE Select	NP_115495.3:p.Asp5422=
XM_017009963.2:c.16287T=	XP_016865452.1:p.Asp5429=
XM_017009964.2:c.16284T=	XP_016865453.1:p.Asp5428=
XM_017009965.1:c.16284T=	XP_016865454.1:p.Asp5428=
XM_017009966.2:c.16206T=	XP_016865455.1:p.Asp5402=
XM_017009967.1:c.16191T=	XP_016865456.1:p.Asp5397=
XM_017009968.2:c.16107T=	XP_016865457.1:p.Asp5369=
XM_017009969.2:c.16287T=	XP_016865458.1:p.Asp5429=
XM_017009972.1:c.9405T=	XP_016865461.1:p.Asp3135=
XM_017009973.1:c.9384T=	XP_016865462.1:p.Asp3128=
NR_003149.2:n.16282T=