Canonical Allele Identifier: CA360367502

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90755183-C-T
• MyVariant Identifiers: chr5:g.90051000C>T (hg19) ; chr5:g.90755183C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755183C>T , CM000667.2:g.90755183C>T	GRCh38
NC_000005.9:g.90051000C>T , CM000667.1:g.90051000C>T	GRCh37
NC_000005.8:g.90086756C>T	NCBI36
NG_007083.1:g.201384C>T
NG_007083.2:g.230840C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11578C>T MANE Select	ENSP00000384582.2:p.Pro3860Ser
ENST00000425867.3:c.709C>T	ENSP00000392618.3:p.Pro237Ser
ENST00000639431.1:c.265+78974C>T	ENSP00000491057.1:n.265+78974C>T
ENST00000640374.1:n.4722C>T
ENST00000640464.1:n.1997C>T
ENST00000405460.6:c.11578C>T	ENSP00000384582.2:p.Pro3860Ser
ENST00000509621.1:c.4275C>T
NM_032119.3:c.11578C>T	NP_115495.3:p.Pro3860Ser
NR_003149.1:n.11591C>T
XM_011543675.1:c.11575C>T	XP_011541977.1:p.Pro3859Ser
XM_011543676.1:c.11497C>T	XP_011541978.1:p.Pro3833Ser
XM_011543677.1:c.8881C>T	XP_011541979.1:p.Pro2961Ser
XM_011543678.1:c.11578C>T	XP_011541980.1:p.Pro3860Ser
NM_032119.4:c.11578C>T MANE Select	NP_115495.3:p.Pro3860Ser
XM_017009963.2:c.11599C>T	XP_016865452.1:p.Pro3867Ser
XM_017009964.2:c.11596C>T	XP_016865453.1:p.Pro3866Ser
XM_017009965.1:c.11596C>T	XP_016865454.1:p.Pro3866Ser
XM_017009966.2:c.11518C>T	XP_016865455.1:p.Pro3840Ser
XM_017009967.1:c.11503C>T	XP_016865456.1:p.Pro3835Ser
XM_017009968.2:c.11599C>T	XP_016865457.1:p.Pro3867Ser
XM_017009969.2:c.11599C>T	XP_016865458.1:p.Pro3867Ser
XM_017009970.2:c.11599C>T	XP_016865459.1:p.Pro3867Ser
XM_017009971.2:c.11599C>T	XP_016865460.1:p.Pro3867Ser
XM_017009972.1:c.4717C>T	XP_016865461.1:p.Pro1573Ser
XM_017009973.1:c.4696C>T	XP_016865462.1:p.Pro1566Ser
NR_003149.2:n.11594C>T