Canonical Allele Identifier: CA360401276

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086924C>T (hg19) ; chr5:g.90791107C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791107C>T , CM000667.2:g.90791107C>T	GRCh38
NC_000005.9:g.90086924C>T , CM000667.1:g.90086924C>T	GRCh37
NC_000005.8:g.90122680C>T	NCBI36
NG_007083.1:g.237308C>T
NG_007083.2:g.266764C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14278C>T MANE Select	ENSP00000384582.2:p.Pro4760Ser
ENST00000425867.3:c.3232C>T	ENSP00000392618.3:p.Pro1078Ser
ENST00000638510.1:n.1545C>T
ENST00000638585.1:n.44C>T
ENST00000638975.1:c.907C>T	ENSP00000492630.1:p.Pro303Ser
ENST00000639431.1:c.265+114898C>T	ENSP00000491057.1:n.265+114898C>T
ENST00000640407.1:c.688C>T	ENSP00000491425.1:p.Pro230Ser
ENST00000405460.6:c.14278C>T	ENSP00000384582.2:p.Pro4760Ser
ENST00000425867.2:c.1261C>T	ENSP00000392618.2:p.Pro421Ser
NM_032119.3:c.14278C>T	NP_115495.3:p.Pro4760Ser
NR_003149.1:n.14291C>T
XM_011543675.1:c.14275C>T	XP_011541977.1:p.Pro4759Ser
XM_011543676.1:c.14197C>T	XP_011541978.1:p.Pro4733Ser
XM_011543677.1:c.11581C>T	XP_011541979.1:p.Pro3861Ser
XM_011543678.1:c.14278C>T	XP_011541980.1:p.Pro4760Ser
NM_032119.4:c.14278C>T MANE Select	NP_115495.3:p.Pro4760Ser
XM_017009963.2:c.14299C>T	XP_016865452.1:p.Pro4767Ser
XM_017009964.2:c.14296C>T	XP_016865453.1:p.Pro4766Ser
XM_017009965.1:c.14296C>T	XP_016865454.1:p.Pro4766Ser
XM_017009966.2:c.14218C>T	XP_016865455.1:p.Pro4740Ser
XM_017009967.1:c.14203C>T	XP_016865456.1:p.Pro4735Ser
XM_017009968.2:c.14299C>T	XP_016865457.1:p.Pro4767Ser
XM_017009969.2:c.14299C>T	XP_016865458.1:p.Pro4767Ser
XM_017009970.2:c.14299C>T	XP_016865459.1:p.Pro4767Ser
XM_017009971.2:c.14299C>T	XP_016865460.1:p.Pro4767Ser
XM_017009972.1:c.7417C>T	XP_016865461.1:p.Pro2473Ser
XM_017009973.1:c.7396C>T	XP_016865462.1:p.Pro2466Ser
NR_003149.2:n.14294C>T