Canonical Allele Identifier: CA445416034

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041432T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745615T>C , CM000667.2:g.90745615T>C	GRCh38
NC_000005.9:g.90041432T>C , CM000667.1:g.90041432T>C	GRCh37
NC_000005.8:g.90077188T>C	NCBI36
NG_007083.1:g.191816T>C
NG_007083.2:g.221272T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10794T>C MANE Select	ENSP00000384582.2:p.Pro3598=
ENST00000639431.1:c.265+69406T>C	ENSP00000491057.1:n.265+69406T>C
ENST00000640374.1:n.3938T>C
ENST00000640464.1:n.1213T>C
ENST00000405460.6:c.10794T>C	ENSP00000384582.2:p.Pro3598=
ENST00000509621.1:c.3491T>C
NM_032119.3:c.10794T>C	NP_115495.3:p.Pro3598=
NR_003149.1:n.10807T>C
XM_011543675.1:c.10791T>C	XP_011541977.1:p.Pro3597=
XM_011543676.1:c.10713T>C	XP_011541978.1:p.Pro3571=
XM_011543677.1:c.8097T>C	XP_011541979.1:p.Pro2699=
XM_011543678.1:c.10794T>C	XP_011541980.1:p.Pro3598=
XM_011543679.1:c.*16T>C	XP_011541981.1:n.*16T>C
NM_032119.4:c.10794T>C MANE Select	NP_115495.3:p.Pro3598=
XM_017009963.2:c.10815T>C	XP_016865452.1:p.Pro3605=
XM_017009964.2:c.10812T>C	XP_016865453.1:p.Pro3604=
XM_017009965.1:c.10812T>C	XP_016865454.1:p.Pro3604=
XM_017009966.2:c.10734T>C	XP_016865455.1:p.Pro3578=
XM_017009967.1:c.10719T>C	XP_016865456.1:p.Pro3573=
XM_017009968.2:c.10815T>C	XP_016865457.1:p.Pro3605=
XM_017009969.2:c.10815T>C	XP_016865458.1:p.Pro3605=
XM_017009970.2:c.10815T>C	XP_016865459.1:p.Pro3605=
XM_017009971.2:c.10815T>C	XP_016865460.1:p.Pro3605=
XM_017009972.1:c.3933T>C	XP_016865461.1:p.Pro1311=
XM_017009973.1:c.3912T>C	XP_016865462.1:p.Pro1304=
XM_017009974.2:c.*16T>C	XP_016865463.1:n.*16T>C
NR_003149.2:n.10810T>C