Canonical Allele Identifier: CA916082742

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90807594T>C , CM000667.2:g.90807594T>C	GRCh38
NC_000005.9:g.90103411T>C , CM000667.1:g.90103411T>C	GRCh37
NC_000005.8:g.90139167T>C	NCBI36
NG_007083.1:g.253795T>C
NG_007083.2:g.283251T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14837-8T>C MANE Select	NP_115495.3:n.14837-8T>C
ENST00000405460.9:c.14837-8T>C MANE Select	ENSP00000384582.2:n.14837-8T>C
NM_032119.3:c.14837-8T>C	NP_115495.3:n.14837-8T>C
NR_003149.1:n.14850-8T>C
NR_003149.2:n.14853-8T>C
ENST00000405460.6:c.14837-8T>C	ENSP00000384582.2:n.14837-8T>C
ENST00000425867.2:c.1820-8T>C	ENSP00000392618.2:n.1820-8T>C
ENST00000425867.3:c.3791-8T>C	ENSP00000392618.3:n.3791-8T>C
ENST00000513828.1:n.533-8T>C
ENST00000638510.1:n.2104-8T>C
ENST00000638585.1:n.428-2639T>C
ENST00000639431.1:c.265+131385T>C	ENSP00000491057.1:n.265+131385T>C
ENST00000640407.1:c.1247-8T>C	ENSP00000491425.1:n.1247-8T>C
XM_011543675.1:c.14834-8T>C	XP_011541977.1:n.14834-8T>C
XM_011543676.1:c.14756-8T>C	XP_011541978.1:n.14756-8T>C
XM_011543677.1:c.12140-8T>C	XP_011541979.1:n.12140-8T>C
XM_011543678.1:c.14837-8T>C	XP_011541980.1:n.14837-8T>C
XM_017009963.2:c.14858-8T>C	XP_016865452.1:n.14858-8T>C
XM_017009964.2:c.14855-8T>C	XP_016865453.1:n.14855-8T>C
XM_017009965.1:c.14855-8T>C	XP_016865454.1:n.14855-8T>C
XM_017009966.2:c.14777-8T>C	XP_016865455.1:n.14777-8T>C
XM_017009967.1:c.14762-8T>C	XP_016865456.1:n.14762-8T>C
XM_017009968.2:c.14683-8T>C	XP_016865457.1:n.14683-8T>C
XM_017009969.2:c.14858-8T>C	XP_016865458.1:n.14858-8T>C
XM_017009970.2:c.14858-8T>C	XP_016865459.1:n.14858-8T>C
XM_017009971.2:c.14683-8T>C	XP_016865460.1:n.14683-8T>C
XM_017009972.1:c.7976-8T>C	XP_016865461.1:n.7976-8T>C
XM_017009973.1:c.7955-8T>C	XP_016865462.1:n.7955-8T>C