Canonical Allele Identifier: CA360409080

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041482C>T (hg19) ; chr5:g.90745665C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745665C>T , CM000667.2:g.90745665C>T	GRCh38
NC_000005.9:g.90041482C>T , CM000667.1:g.90041482C>T	GRCh37
NC_000005.8:g.90077238C>T	NCBI36
NG_007083.1:g.191866C>T
NG_007083.2:g.221322C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10844C>T MANE Select	ENSP00000384582.2:p.Pro3615Leu
ENST00000639431.1:c.265+69456C>T	ENSP00000491057.1:n.265+69456C>T
ENST00000640374.1:n.3988C>T
ENST00000640464.1:n.1263C>T
ENST00000405460.6:c.10844C>T	ENSP00000384582.2:p.Pro3615Leu
ENST00000509621.1:c.3541C>T
NM_032119.3:c.10844C>T	NP_115495.3:p.Pro3615Leu
NR_003149.1:n.10857C>T
XM_011543675.1:c.10841C>T	XP_011541977.1:p.Pro3614Leu
XM_011543676.1:c.10763C>T	XP_011541978.1:p.Pro3588Leu
XM_011543677.1:c.8147C>T	XP_011541979.1:p.Pro2716Leu
XM_011543678.1:c.10844C>T	XP_011541980.1:p.Pro3615Leu
XM_011543679.1:c.*66C>T	XP_011541981.1:n.*66C>T
NM_032119.4:c.10844C>T MANE Select	NP_115495.3:p.Pro3615Leu
XM_017009963.2:c.10865C>T	XP_016865452.1:p.Pro3622Leu
XM_017009964.2:c.10862C>T	XP_016865453.1:p.Pro3621Leu
XM_017009965.1:c.10862C>T	XP_016865454.1:p.Pro3621Leu
XM_017009966.2:c.10784C>T	XP_016865455.1:p.Pro3595Leu
XM_017009967.1:c.10769C>T	XP_016865456.1:p.Pro3590Leu
XM_017009968.2:c.10865C>T	XP_016865457.1:p.Pro3622Leu
XM_017009969.2:c.10865C>T	XP_016865458.1:p.Pro3622Leu
XM_017009970.2:c.10865C>T	XP_016865459.1:p.Pro3622Leu
XM_017009971.2:c.10865C>T	XP_016865460.1:p.Pro3622Leu
XM_017009972.1:c.3983C>T	XP_016865461.1:p.Pro1328Leu
XM_017009973.1:c.3962C>T	XP_016865462.1:p.Pro1321Leu
XM_017009974.2:c.*66C>T	XP_016865463.1:n.*66C>T
NR_003149.2:n.10860C>T