Canonical Allele Identifier: CA1562873607

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725711T= , CM000667.2:g.90725711T=	GRCh38
NC_000005.9:g.90021528T= , CM000667.1:g.90021528T=	GRCh37
NC_000005.8:g.90057284T=	NCBI36
NG_007083.1:g.171912T=
NG_007083.2:g.201368T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10161+55T= MANE Select	ENSP00000384582.2:n.10161+55T=
ENST00000639431.1:c.265+49502T=	ENSP00000491057.1:n.265+49502T=
ENST00000640374.1:n.3305+55T=
ENST00000640464.1:n.580+55T=
ENST00000405460.6:c.10161+55T=	ENSP00000384582.2:n.10161+55T=
ENST00000509621.1:c.2858+55T=
NM_032119.3:c.10161+55T=	NP_115495.3:n.10161+55T=
NR_003149.1:n.10174+55T=
XM_011543675.1:c.10158+55T=	XP_011541977.1:n.10158+55T=
XM_011543676.1:c.10080+55T=	XP_011541978.1:n.10080+55T=
XM_011543677.1:c.7464+55T=	XP_011541979.1:n.7464+55T=
XM_011543678.1:c.10161+55T=	XP_011541980.1:n.10161+55T=
XM_011543679.1:c.10161+55T=	XP_011541981.1:n.10161+55T=
XR_948560.1:n.272-9902A=
NM_032119.4:c.10161+55T= MANE Select	NP_115495.3:n.10161+55T=
XM_017009963.2:c.10182+55T=	XP_016865452.1:n.10182+55T=
XM_017009964.2:c.10179+55T=	XP_016865453.1:n.10179+55T=
XM_017009965.1:c.10179+55T=	XP_016865454.1:n.10179+55T=
XM_017009966.2:c.10101+55T=	XP_016865455.1:n.10101+55T=
XM_017009967.1:c.10086+55T=	XP_016865456.1:n.10086+55T=
XM_017009968.2:c.10182+55T=	XP_016865457.1:n.10182+55T=
XM_017009969.2:c.10182+55T=	XP_016865458.1:n.10182+55T=
XM_017009970.2:c.10182+55T=	XP_016865459.1:n.10182+55T=
XM_017009971.2:c.10182+55T=	XP_016865460.1:n.10182+55T=
XM_017009972.1:c.3300+55T=	XP_016865461.1:n.3300+55T=
XM_017009973.1:c.3279+55T=	XP_016865462.1:n.3279+55T=
XM_017009974.2:c.10182+55T=	XP_016865463.1:n.10182+55T=
XR_001742802.1:n.2523-9902A=
NR_003149.2:n.10177+55T=