Canonical Allele Identifier: CA1078677453

Gene: ADGRV1

Linked Data

• dbSNP Id: rs749743624
• gnomAD v3: 5-90728947-G-T
• gnomAD v4: 5-90728947-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728947G>T , CM000667.2:g.90728947G>T	GRCh38
NC_000005.9:g.90024764G>T , CM000667.1:g.90024764G>T	GRCh37
NC_000005.8:g.90060520G>T	NCBI36
NG_007083.1:g.175148G>T
NG_007083.2:g.204604G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10426+14G>T MANE Select	ENSP00000384582.2:n.10426+14G>T
ENST00000639431.1:c.265+52738G>T	ENSP00000491057.1:n.265+52738G>T
ENST00000640374.1:n.3570+14G>T
ENST00000640464.1:n.845+14G>T
ENST00000405460.6:c.10426+14G>T	ENSP00000384582.2:n.10426+14G>T
ENST00000509621.1:c.3123+14G>T
NM_032119.3:c.10426+14G>T	NP_115495.3:n.10426+14G>T
NR_003149.1:n.10439+14G>T
XM_011543675.1:c.10423+14G>T	XP_011541977.1:n.10423+14G>T
XM_011543676.1:c.10345+14G>T	XP_011541978.1:n.10345+14G>T
XM_011543677.1:c.7729+14G>T	XP_011541979.1:n.7729+14G>T
XM_011543678.1:c.10426+14G>T	XP_011541980.1:n.10426+14G>T
XM_011543679.1:c.10426+14G>T	XP_011541981.1:n.10426+14G>T
XR_948560.1:n.271+11960C>A
NM_032119.4:c.10426+14G>T MANE Select	NP_115495.3:n.10426+14G>T
XM_017009963.2:c.10447+14G>T	XP_016865452.1:n.10447+14G>T
XM_017009964.2:c.10444+14G>T	XP_016865453.1:n.10444+14G>T
XM_017009965.1:c.10444+14G>T	XP_016865454.1:n.10444+14G>T
XM_017009966.2:c.10366+14G>T	XP_016865455.1:n.10366+14G>T
XM_017009967.1:c.10351+14G>T	XP_016865456.1:n.10351+14G>T
XM_017009968.2:c.10447+14G>T	XP_016865457.1:n.10447+14G>T
XM_017009969.2:c.10447+14G>T	XP_016865458.1:n.10447+14G>T
XM_017009970.2:c.10447+14G>T	XP_016865459.1:n.10447+14G>T
XM_017009971.2:c.10447+14G>T	XP_016865460.1:n.10447+14G>T
XM_017009972.1:c.3565+14G>T	XP_016865461.1:n.3565+14G>T
XM_017009973.1:c.3544+14G>T	XP_016865462.1:n.3544+14G>T
XM_017009974.2:c.10447+14G>T	XP_016865463.1:n.10447+14G>T
XR_001742802.1:n.2522+11960C>A
NR_003149.2:n.10442+14G>T