Canonical Allele Identifier: CA121825026

Gene: ADGRV1

Linked Data

• dbSNP Id: rs565248021
• gnomAD v2: 5-89922916-G-T
• gnomAD v3: 5-90627099-G-T
• gnomAD v4: 5-90627099-G-T
• MyVariant Identifiers: chr5:g.89922916G>T (hg19) ; chr5:g.90627099G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627099G>T , CM000667.2:g.90627099G>T	GRCh38
NC_000005.9:g.89922916G>T , CM000667.1:g.89922916G>T	GRCh37
NC_000005.8:g.89958672G>T	NCBI36
NG_007083.1:g.73300G>T
NG_007083.2:g.102756G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.673-112G>T MANE Select	ENSP00000384582.2:n.673-112G>T
ENST00000640083.1:n.378-112G>T
ENST00000640109.1:n.769-112G>T
ENST00000640281.1:n.732-112G>T
ENST00000405460.6:c.673-112G>T	ENSP00000384582.2:n.673-112G>T
NM_032119.3:c.673-112G>T	NP_115495.3:n.673-112G>T
NR_003149.1:n.769-112G>T
XM_011543675.1:c.673-112G>T	XP_011541977.1:n.673-112G>T
XM_011543676.1:c.673-112G>T	XP_011541978.1:n.673-112G>T
XM_011543678.1:c.673-112G>T	XP_011541980.1:n.673-112G>T
XM_011543679.1:c.673-112G>T	XP_011541981.1:n.673-112G>T
NM_032119.4:c.673-112G>T MANE Select	NP_115495.3:n.673-112G>T
XM_017009963.2:c.673-112G>T	XP_016865452.1:n.673-112G>T
XM_017009964.2:c.673-112G>T	XP_016865453.1:n.673-112G>T
XM_017009965.1:c.670-112G>T	XP_016865454.1:n.670-112G>T
XM_017009966.2:c.673-112G>T	XP_016865455.1:n.673-112G>T
XM_017009967.1:c.577-112G>T	XP_016865456.1:n.577-112G>T
XM_017009968.2:c.673-112G>T	XP_016865457.1:n.673-112G>T
XM_017009969.2:c.673-112G>T	XP_016865458.1:n.673-112G>T
XM_017009970.2:c.673-112G>T	XP_016865459.1:n.673-112G>T
XM_017009971.2:c.673-112G>T	XP_016865460.1:n.673-112G>T
XM_017009974.2:c.673-112G>T	XP_016865463.1:n.673-112G>T
NR_003149.2:n.772-112G>T