Canonical Allele Identifier: CA360365940

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89923160A>C (hg19) ; chr5:g.90627343A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627343A>C , CM000667.2:g.90627343A>C	GRCh38
NC_000005.9:g.89923160A>C , CM000667.1:g.89923160A>C	GRCh37
NC_000005.8:g.89958916A>C	NCBI36
NG_007083.1:g.73544A>C
NG_007083.2:g.103000A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.805A>C MANE Select	ENSP00000384582.2:p.Ile269Leu
ENST00000640083.1:n.510A>C
ENST00000640109.1:n.901A>C
ENST00000640281.1:n.864A>C
ENST00000405460.6:c.805A>C	ENSP00000384582.2:p.Ile269Leu
NM_032119.3:c.805A>C	NP_115495.3:p.Ile269Leu
NR_003149.1:n.901A>C
XM_011543675.1:c.805A>C	XP_011541977.1:p.Ile269Leu
XM_011543676.1:c.805A>C	XP_011541978.1:p.Ile269Leu
XM_011543678.1:c.805A>C	XP_011541980.1:p.Ile269Leu
XM_011543679.1:c.805A>C	XP_011541981.1:p.Ile269Leu
NM_032119.4:c.805A>C MANE Select	NP_115495.3:p.Ile269Leu
XM_017009963.2:c.805A>C	XP_016865452.1:p.Ile269Leu
XM_017009964.2:c.805A>C	XP_016865453.1:p.Ile269Leu
XM_017009965.1:c.802A>C	XP_016865454.1:p.Ile268Leu
XM_017009966.2:c.805A>C	XP_016865455.1:p.Ile269Leu
XM_017009967.1:c.709A>C	XP_016865456.1:p.Ile237Leu
XM_017009968.2:c.805A>C	XP_016865457.1:p.Ile269Leu
XM_017009969.2:c.805A>C	XP_016865458.1:p.Ile269Leu
XM_017009970.2:c.805A>C	XP_016865459.1:p.Ile269Leu
XM_017009971.2:c.805A>C	XP_016865460.1:p.Ile269Leu
XM_017009974.2:c.805A>C	XP_016865463.1:p.Ile269Leu
NR_003149.2:n.904A>C