Canonical Allele Identifier: CA1562870623

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716666T= , CM000667.2:g.90716666T=	GRCh38
NC_000005.9:g.90012483T= , CM000667.1:g.90012483T=	GRCh37
NC_000005.8:g.90048239T=	NCBI36
NG_007083.1:g.162867T=
NG_007083.2:g.192323T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9384T= MANE Select	ENSP00000384582.2:p.Asn3128=
ENST00000639431.1:c.265+40457T=	ENSP00000491057.1:n.265+40457T=
ENST00000639473.1:n.4843T=
ENST00000640012.1:c.3191T=
ENST00000640374.1:n.2528T=
ENST00000640779.1:c.4113T=
ENST00000405460.6:c.9384T=	ENSP00000384582.2:p.Asn3128=
ENST00000509621.1:c.2081T=
NM_032119.3:c.9384T=	NP_115495.3:p.Asn3128=
NR_003149.1:n.9397T=
XM_011543675.1:c.9381T=	XP_011541977.1:p.Asn3127=
XM_011543676.1:c.9303T=	XP_011541978.1:p.Asn3101=
XM_011543677.1:c.6687T=	XP_011541979.1:p.Asn2229=
XM_011543678.1:c.9384T=	XP_011541980.1:p.Asn3128=
XM_011543679.1:c.9384T=	XP_011541981.1:p.Asn3128=
XR_948560.1:n.272-857A=
NM_032119.4:c.9384T= MANE Select	NP_115495.3:p.Asn3128=
XM_017009963.2:c.9405T=	XP_016865452.1:p.Asn3135=
XM_017009964.2:c.9402T=	XP_016865453.1:p.Asn3134=
XM_017009965.1:c.9402T=	XP_016865454.1:p.Asn3134=
XM_017009966.2:c.9324T=	XP_016865455.1:p.Asn3108=
XM_017009967.1:c.9309T=	XP_016865456.1:p.Asn3103=
XM_017009968.2:c.9405T=	XP_016865457.1:p.Asn3135=
XM_017009969.2:c.9405T=	XP_016865458.1:p.Asn3135=
XM_017009970.2:c.9405T=	XP_016865459.1:p.Asn3135=
XM_017009971.2:c.9405T=	XP_016865460.1:p.Asn3135=
XM_017009972.1:c.2523T=	XP_016865461.1:p.Asn841=
XM_017009973.1:c.2502T=	XP_016865462.1:p.Asn834=
XM_017009974.2:c.9405T=	XP_016865463.1:p.Asn3135=
XR_001742802.1:n.2523-857A=
NR_003149.2:n.9400T=