Canonical Allele Identifier: CA360391347

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89940686G>C (hg19) ; chr5:g.90644869G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644869G>C , CM000667.2:g.90644869G>C	GRCh38
NC_000005.9:g.89940686G>C , CM000667.1:g.89940686G>C	GRCh37
NC_000005.8:g.89976442G>C	NCBI36
NG_007083.1:g.91070G>C
NG_007083.2:g.120526G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2898G>C MANE Select	ENSP00000384582.2:p.Glu966Asp
ENST00000504142.2:n.1664G>C
ENST00000639676.1:n.496G>C
ENST00000640403.1:c.201G>C	ENSP00000492531.1:p.Glu67Asp
ENST00000405460.6:c.2898G>C	ENSP00000384582.2:p.Glu966Asp
ENST00000504142.1:c.1663G>C
NM_032119.3:c.2898G>C	NP_115495.3:p.Glu966Asp
NR_003149.1:n.2994G>C
XM_011543675.1:c.2898G>C	XP_011541977.1:p.Glu966Asp
XM_011543676.1:c.2898G>C	XP_011541978.1:p.Glu966Asp
XM_011543677.1:c.201G>C	XP_011541979.1:p.Glu67Asp
XM_011543678.1:c.2898G>C	XP_011541980.1:p.Glu966Asp
XM_011543679.1:c.2898G>C	XP_011541981.1:p.Glu966Asp
NM_032119.4:c.2898G>C MANE Select	NP_115495.3:p.Glu966Asp
XM_017009963.2:c.2898G>C	XP_016865452.1:p.Glu966Asp
XM_017009964.2:c.2898G>C	XP_016865453.1:p.Glu966Asp
XM_017009965.1:c.2895G>C	XP_016865454.1:p.Glu965Asp
XM_017009966.2:c.2898G>C	XP_016865455.1:p.Glu966Asp
XM_017009967.1:c.2802G>C	XP_016865456.1:p.Glu934Asp
XM_017009968.2:c.2898G>C	XP_016865457.1:p.Glu966Asp
XM_017009969.2:c.2898G>C	XP_016865458.1:p.Glu966Asp
XM_017009970.2:c.2898G>C	XP_016865459.1:p.Glu966Asp
XM_017009971.2:c.2898G>C	XP_016865460.1:p.Glu966Asp
XM_017009974.2:c.2898G>C	XP_016865463.1:p.Glu966Asp
NR_003149.2:n.2997G>C