Canonical Allele Identifier: CA2674563687

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90644879-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644879G>T , CM000667.2:g.90644879G>T	GRCh38
NC_000005.9:g.89940696G>T , CM000667.1:g.89940696G>T	GRCh37
NC_000005.8:g.89976452G>T	NCBI36
NG_007083.1:g.91080G>T
NG_007083.2:g.120536G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2898+10G>T MANE Select	ENSP00000384582.2:n.2898+10G>T
ENST00000504142.2:n.1664+10G>T
ENST00000639676.1:n.496+10G>T
ENST00000640403.1:c.201+10G>T	ENSP00000492531.1:n.201+10G>T
ENST00000405460.6:c.2898+10G>T	ENSP00000384582.2:n.2898+10G>T
ENST00000504142.1:c.1663+10G>T
NM_032119.3:c.2898+10G>T	NP_115495.3:n.2898+10G>T
NR_003149.1:n.2994+10G>T
XM_011543675.1:c.2898+10G>T	XP_011541977.1:n.2898+10G>T
XM_011543676.1:c.2898+10G>T	XP_011541978.1:n.2898+10G>T
XM_011543677.1:c.201+10G>T	XP_011541979.1:n.201+10G>T
XM_011543678.1:c.2898+10G>T	XP_011541980.1:n.2898+10G>T
XM_011543679.1:c.2898+10G>T	XP_011541981.1:n.2898+10G>T
NM_032119.4:c.2898+10G>T MANE Select	NP_115495.3:n.2898+10G>T
XM_017009963.2:c.2898+10G>T	XP_016865452.1:n.2898+10G>T
XM_017009964.2:c.2898+10G>T	XP_016865453.1:n.2898+10G>T
XM_017009965.1:c.2895+10G>T	XP_016865454.1:n.2895+10G>T
XM_017009966.2:c.2898+10G>T	XP_016865455.1:n.2898+10G>T
XM_017009967.1:c.2802+10G>T	XP_016865456.1:n.2802+10G>T
XM_017009968.2:c.2898+10G>T	XP_016865457.1:n.2898+10G>T
XM_017009969.2:c.2898+10G>T	XP_016865458.1:n.2898+10G>T
XM_017009970.2:c.2898+10G>T	XP_016865459.1:n.2898+10G>T
XM_017009971.2:c.2898+10G>T	XP_016865460.1:n.2898+10G>T
XM_017009974.2:c.2898+10G>T	XP_016865463.1:n.2898+10G>T
NR_003149.2:n.2997+10G>T