Canonical Allele Identifier: CA445415143

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90024716T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728899T>C , CM000667.2:g.90728899T>C	GRCh38
NC_000005.9:g.90024716T>C , CM000667.1:g.90024716T>C	GRCh37
NC_000005.8:g.90060472T>C	NCBI36
NG_007083.1:g.175100T>C
NG_007083.2:g.204556T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10392T>C MANE Select	ENSP00000384582.2:p.Asp3464=
ENST00000639431.1:c.265+52690T>C	ENSP00000491057.1:n.265+52690T>C
ENST00000640374.1:n.3536T>C
ENST00000640464.1:n.811T>C
ENST00000405460.6:c.10392T>C	ENSP00000384582.2:p.Asp3464=
ENST00000509621.1:c.3089T>C
NM_032119.3:c.10392T>C	NP_115495.3:p.Asp3464=
NR_003149.1:n.10405T>C
XM_011543675.1:c.10389T>C	XP_011541977.1:p.Asp3463=
XM_011543676.1:c.10311T>C	XP_011541978.1:p.Asp3437=
XM_011543677.1:c.7695T>C	XP_011541979.1:p.Asp2565=
XM_011543678.1:c.10392T>C	XP_011541980.1:p.Asp3464=
XM_011543679.1:c.10392T>C	XP_011541981.1:p.Asp3464=
XR_948560.1:n.271+12008A>G
NM_032119.4:c.10392T>C MANE Select	NP_115495.3:p.Asp3464=
XM_017009963.2:c.10413T>C	XP_016865452.1:p.Asp3471=
XM_017009964.2:c.10410T>C	XP_016865453.1:p.Asp3470=
XM_017009965.1:c.10410T>C	XP_016865454.1:p.Asp3470=
XM_017009966.2:c.10332T>C	XP_016865455.1:p.Asp3444=
XM_017009967.1:c.10317T>C	XP_016865456.1:p.Asp3439=
XM_017009968.2:c.10413T>C	XP_016865457.1:p.Asp3471=
XM_017009969.2:c.10413T>C	XP_016865458.1:p.Asp3471=
XM_017009970.2:c.10413T>C	XP_016865459.1:p.Asp3471=
XM_017009971.2:c.10413T>C	XP_016865460.1:p.Asp3471=
XM_017009972.1:c.3531T>C	XP_016865461.1:p.Asp1177=
XM_017009973.1:c.3510T>C	XP_016865462.1:p.Asp1170=
XM_017009974.2:c.10413T>C	XP_016865463.1:p.Asp3471=
XR_001742802.1:n.2522+12008A>G
NR_003149.2:n.10408T>C