Canonical Allele Identifier: CA1562918301

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823548A= , CM000667.2:g.90823548A=	GRCh38
NC_000005.9:g.90119365A= , CM000667.1:g.90119365A=	GRCh37
NC_000005.8:g.90155121A=	NCBI36
NG_007083.1:g.269749A=
NG_007083.2:g.299205A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16320A= MANE Select	ENSP00000384582.2:p.Thr5440=
ENST00000425867.3:c.5274A=	ENSP00000392618.3:p.Thr1758=
ENST00000638510.1:n.3587A=
ENST00000639431.1:c.265+147339A=	ENSP00000491057.1:n.265+147339A=
ENST00000640061.1:n.128+1366A=
ENST00000640407.1:c.2730A=	ENSP00000491425.1:p.Thr910=
ENST00000405460.6:c.16320A=	ENSP00000384582.2:p.Thr5440=
ENST00000425867.2:c.3303A=	ENSP00000392618.2:p.Thr1101=
NM_032119.3:c.16320A=	NP_115495.3:p.Thr5440=
NR_003149.1:n.16333A=
XM_011543675.1:c.16317A=	XP_011541977.1:p.Thr5439=
XM_011543676.1:c.16239A=	XP_011541978.1:p.Thr5413=
XM_011543677.1:c.13623A=	XP_011541979.1:p.Thr4541=
NM_032119.4:c.16320A= MANE Select	NP_115495.3:p.Thr5440=
XM_017009963.2:c.16341A=	XP_016865452.1:p.Thr5447=
XM_017009964.2:c.16338A=	XP_016865453.1:p.Thr5446=
XM_017009965.1:c.16338A=	XP_016865454.1:p.Thr5446=
XM_017009966.2:c.16260A=	XP_016865455.1:p.Thr5420=
XM_017009967.1:c.16245A=	XP_016865456.1:p.Thr5415=
XM_017009968.2:c.16161A=	XP_016865457.1:p.Thr5387=
XM_017009969.2:c.16341A=	XP_016865458.1:p.Thr5447=
XM_017009972.1:c.9459A=	XP_016865461.1:p.Thr3153=
XM_017009973.1:c.9438A=	XP_016865462.1:p.Thr3146=
NR_003149.2:n.16336A=