Canonical Allele Identifier: CA445465703

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923312T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627495T>C , CM000667.2:g.90627495T>C	GRCh38
NC_000005.9:g.89923312T>C , CM000667.1:g.89923312T>C	GRCh37
NC_000005.8:g.89959068T>C	NCBI36
NG_007083.1:g.73696T>C
NG_007083.2:g.103152T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.957T>C MANE Select	ENSP00000384582.2:p.Asn319=
ENST00000640083.1:n.662T>C
ENST00000640109.1:n.1053T>C
ENST00000640281.1:n.1016T>C
ENST00000405460.6:c.957T>C	ENSP00000384582.2:p.Asn319=
NM_032119.3:c.957T>C	NP_115495.3:p.Asn319=
NR_003149.1:n.1053T>C
XM_011543675.1:c.957T>C	XP_011541977.1:p.Asn319=
XM_011543676.1:c.957T>C	XP_011541978.1:p.Asn319=
XM_011543678.1:c.957T>C	XP_011541980.1:p.Asn319=
XM_011543679.1:c.957T>C	XP_011541981.1:p.Asn319=
NM_032119.4:c.957T>C MANE Select	NP_115495.3:p.Asn319=
XM_017009963.2:c.957T>C	XP_016865452.1:p.Asn319=
XM_017009964.2:c.957T>C	XP_016865453.1:p.Asn319=
XM_017009965.1:c.954T>C	XP_016865454.1:p.Asn318=
XM_017009966.2:c.957T>C	XP_016865455.1:p.Asn319=
XM_017009967.1:c.861T>C	XP_016865456.1:p.Asn287=
XM_017009968.2:c.957T>C	XP_016865457.1:p.Asn319=
XM_017009969.2:c.957T>C	XP_016865458.1:p.Asn319=
XM_017009970.2:c.957T>C	XP_016865459.1:p.Asn319=
XM_017009971.2:c.957T>C	XP_016865460.1:p.Asn319=
XM_017009974.2:c.957T>C	XP_016865463.1:p.Asn319=
NR_003149.2:n.1056T>C