Canonical Allele Identifier: CA560901659

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1307666318
• gnomAD v2: 5-90021293-T-G
• MyVariant Identifiers: chr5:g.90021293T>G (hg19) ; chr5:g.90725476T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725476T>G , CM000667.2:g.90725476T>G	GRCh38
NC_000005.9:g.90021293T>G , CM000667.1:g.90021293T>G	GRCh37
NC_000005.8:g.90057049T>G	NCBI36
NG_007083.1:g.171677T>G
NG_007083.2:g.201133T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10054-73T>G MANE Select	ENSP00000384582.2:n.10054-73T>G
ENST00000639431.1:c.265+49267T>G	ENSP00000491057.1:n.265+49267T>G
ENST00000640374.1:n.3198-73T>G
ENST00000640464.1:n.473-73T>G
ENST00000405460.6:c.10054-73T>G	ENSP00000384582.2:n.10054-73T>G
ENST00000509621.1:c.2751-73T>G
NM_032119.3:c.10054-73T>G	NP_115495.3:n.10054-73T>G
NR_003149.1:n.10067-73T>G
XM_011543675.1:c.10051-73T>G	XP_011541977.1:n.10051-73T>G
XM_011543676.1:c.9973-73T>G	XP_011541978.1:n.9973-73T>G
XM_011543677.1:c.7357-73T>G	XP_011541979.1:n.7357-73T>G
XM_011543678.1:c.10054-73T>G	XP_011541980.1:n.10054-73T>G
XM_011543679.1:c.10054-73T>G	XP_011541981.1:n.10054-73T>G
XR_948560.1:n.272-9667A>C
NM_032119.4:c.10054-73T>G MANE Select	NP_115495.3:n.10054-73T>G
XM_017009963.2:c.10075-73T>G	XP_016865452.1:n.10075-73T>G
XM_017009964.2:c.10072-73T>G	XP_016865453.1:n.10072-73T>G
XM_017009965.1:c.10072-73T>G	XP_016865454.1:n.10072-73T>G
XM_017009966.2:c.9994-73T>G	XP_016865455.1:n.9994-73T>G
XM_017009967.1:c.9979-73T>G	XP_016865456.1:n.9979-73T>G
XM_017009968.2:c.10075-73T>G	XP_016865457.1:n.10075-73T>G
XM_017009969.2:c.10075-73T>G	XP_016865458.1:n.10075-73T>G
XM_017009970.2:c.10075-73T>G	XP_016865459.1:n.10075-73T>G
XM_017009971.2:c.10075-73T>G	XP_016865460.1:n.10075-73T>G
XM_017009972.1:c.3193-73T>G	XP_016865461.1:n.3193-73T>G
XM_017009973.1:c.3172-73T>G	XP_016865462.1:n.3172-73T>G
XM_017009974.2:c.10075-73T>G	XP_016865463.1:n.10075-73T>G
XR_001742802.1:n.2523-9667A>C
NR_003149.2:n.10070-73T>G