Canonical Allele Identifier: CA445436617

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119407A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823590A>C , CM000667.2:g.90823590A>C	GRCh38
NC_000005.9:g.90119407A>C , CM000667.1:g.90119407A>C	GRCh37
NC_000005.8:g.90155163A>C	NCBI36
NG_007083.1:g.269791A>C
NG_007083.2:g.299247A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16362A>C MANE Select	ENSP00000384582.2:p.Pro5454=
ENST00000425867.3:c.5316A>C	ENSP00000392618.3:p.Pro1772=
ENST00000638510.1:n.3629A>C
ENST00000639431.1:c.265+147381A>C	ENSP00000491057.1:n.265+147381A>C
ENST00000640061.1:n.128+1408A>C
ENST00000640407.1:c.2772A>C	ENSP00000491425.1:p.Pro924=
ENST00000405460.6:c.16362A>C	ENSP00000384582.2:p.Pro5454=
ENST00000425867.2:c.3345A>C	ENSP00000392618.2:p.Pro1115=
NM_032119.3:c.16362A>C	NP_115495.3:p.Pro5454=
NR_003149.1:n.16375A>C
XM_011543675.1:c.16359A>C	XP_011541977.1:p.Pro5453=
XM_011543676.1:c.16281A>C	XP_011541978.1:p.Pro5427=
XM_011543677.1:c.13665A>C	XP_011541979.1:p.Pro4555=
NM_032119.4:c.16362A>C MANE Select	NP_115495.3:p.Pro5454=
XM_017009963.2:c.16383A>C	XP_016865452.1:p.Pro5461=
XM_017009964.2:c.16380A>C	XP_016865453.1:p.Pro5460=
XM_017009965.1:c.16380A>C	XP_016865454.1:p.Pro5460=
XM_017009966.2:c.16302A>C	XP_016865455.1:p.Pro5434=
XM_017009967.1:c.16287A>C	XP_016865456.1:p.Pro5429=
XM_017009968.2:c.16203A>C	XP_016865457.1:p.Pro5401=
XM_017009969.2:c.16383A>C	XP_016865458.1:p.Pro5461=
XM_017009972.1:c.9501A>C	XP_016865461.1:p.Pro3167=
XM_017009973.1:c.9480A>C	XP_016865462.1:p.Pro3160=
NR_003149.2:n.16378A>C