Canonical Allele Identifier: CA445415102

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90024671T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728854T>A , CM000667.2:g.90728854T>A	GRCh38
NC_000005.9:g.90024671T>A , CM000667.1:g.90024671T>A	GRCh37
NC_000005.8:g.90060427T>A	NCBI36
NG_007083.1:g.175055T>A
NG_007083.2:g.204511T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10347T>A MANE Select	ENSP00000384582.2:p.Pro3449=
ENST00000639431.1:c.265+52645T>A	ENSP00000491057.1:n.265+52645T>A
ENST00000640374.1:n.3491T>A
ENST00000640464.1:n.766T>A
ENST00000405460.6:c.10347T>A	ENSP00000384582.2:p.Pro3449=
ENST00000509621.1:c.3044T>A
NM_032119.3:c.10347T>A	NP_115495.3:p.Pro3449=
NR_003149.1:n.10360T>A
XM_011543675.1:c.10344T>A	XP_011541977.1:p.Pro3448=
XM_011543676.1:c.10266T>A	XP_011541978.1:p.Pro3422=
XM_011543677.1:c.7650T>A	XP_011541979.1:p.Pro2550=
XM_011543678.1:c.10347T>A	XP_011541980.1:p.Pro3449=
XM_011543679.1:c.10347T>A	XP_011541981.1:p.Pro3449=
XR_948560.1:n.271+12053A>T
NM_032119.4:c.10347T>A MANE Select	NP_115495.3:p.Pro3449=
XM_017009963.2:c.10368T>A	XP_016865452.1:p.Pro3456=
XM_017009964.2:c.10365T>A	XP_016865453.1:p.Pro3455=
XM_017009965.1:c.10365T>A	XP_016865454.1:p.Pro3455=
XM_017009966.2:c.10287T>A	XP_016865455.1:p.Pro3429=
XM_017009967.1:c.10272T>A	XP_016865456.1:p.Pro3424=
XM_017009968.2:c.10368T>A	XP_016865457.1:p.Pro3456=
XM_017009969.2:c.10368T>A	XP_016865458.1:p.Pro3456=
XM_017009970.2:c.10368T>A	XP_016865459.1:p.Pro3456=
XM_017009971.2:c.10368T>A	XP_016865460.1:p.Pro3456=
XM_017009972.1:c.3486T>A	XP_016865461.1:p.Pro1162=
XM_017009973.1:c.3465T>A	XP_016865462.1:p.Pro1155=
XM_017009974.2:c.10368T>A	XP_016865463.1:p.Pro3456=
XR_001742802.1:n.2522+12053A>T
NR_003149.2:n.10363T>A