Canonical Allele Identifier: CA3342401

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90855737C>T , CM000667.2:g.90855737C>T	GRCh38
NC_000005.9:g.90151554C>T , CM000667.1:g.90151554C>T	GRCh37
NC_000005.8:g.90187310C>T	NCBI36
NG_007083.1:g.301938C>T
NG_007083.2:g.331394C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17595-4C>T MANE Select	NP_115495.3:n.17595-4C>T
ENST00000405460.9:c.17595-4C>T MANE Select	ENSP00000384582.2:n.17595-4C>T
NM_032119.3:c.17595-4C>T	NP_115495.3:n.17595-4C>T
NR_003149.1:n.17608-4C>T
NR_003149.2:n.17611-4C>T
ENST00000405460.6:c.17595-4C>T	ENSP00000384582.2:n.17595-4C>T
ENST00000425867.2:c.4578-4C>T	ENSP00000392618.2:n.4578-4C>T
ENST00000425867.3:c.6549-4C>T	ENSP00000392618.3:n.6549-4C>T
ENST00000503852.1:n.143-4C>T
ENST00000638510.1:n.4862-4C>T
ENST00000638990.1:c.807-4C>T
ENST00000639431.1:c.266-129607C>T	ENSP00000491057.1:n.266-129607C>T
ENST00000640407.1:c.4044-4C>T	ENSP00000491425.1:n.4044-4C>T
XM_011543675.1:c.17592-4C>T	XP_011541977.1:n.17592-4C>T
XM_011543676.1:c.17514-4C>T	XP_011541978.1:n.17514-4C>T
XM_011543677.1:c.14898-4C>T	XP_011541979.1:n.14898-4C>T
XM_017009963.2:c.17616-4C>T	XP_016865452.1:n.17616-4C>T
XM_017009964.2:c.17613-4C>T	XP_016865453.1:n.17613-4C>T
XM_017009965.1:c.17613-4C>T	XP_016865454.1:n.17613-4C>T
XM_017009966.2:c.17535-4C>T	XP_016865455.1:n.17535-4C>T
XM_017009967.1:c.17520-4C>T	XP_016865456.1:n.17520-4C>T
XM_017009968.2:c.17436-4C>T	XP_016865457.1:n.17436-4C>T
XM_017009969.2:c.17616-4C>T	XP_016865458.1:n.17616-4C>T
XM_017009972.1:c.10734-4C>T	XP_016865461.1:n.10734-4C>T
XM_017009973.1:c.10713-4C>T	XP_016865462.1:n.10713-4C>T