Canonical Allele Identifier: CA360396209

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008147T>C (hg19) ; chr5:g.90712330T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712330T>C , CM000667.2:g.90712330T>C	GRCh38
NC_000005.9:g.90008147T>C , CM000667.1:g.90008147T>C	GRCh37
NC_000005.8:g.90043903T>C	NCBI36
NG_007083.1:g.158531T>C
NG_007083.2:g.187987T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9086T>C MANE Select	ENSP00000384582.2:p.Ile3029Thr
ENST00000639431.1:c.265+36121T>C	ENSP00000491057.1:n.265+36121T>C
ENST00000639473.1:n.4545T>C
ENST00000640012.1:c.2893T>C
ENST00000640374.1:n.2230T>C
ENST00000640779.1:c.3815T>C
ENST00000405460.6:c.9086T>C	ENSP00000384582.2:p.Ile3029Thr
ENST00000509621.1:c.1783T>C
NM_032119.3:c.9086T>C	NP_115495.3:p.Ile3029Thr
NR_003149.1:n.9099T>C
XM_011543675.1:c.9083T>C	XP_011541977.1:p.Ile3028Thr
XM_011543676.1:c.9005T>C	XP_011541978.1:p.Ile3002Thr
XM_011543677.1:c.6389T>C	XP_011541979.1:p.Ile2130Thr
XM_011543678.1:c.9086T>C	XP_011541980.1:p.Ile3029Thr
XM_011543679.1:c.9086T>C	XP_011541981.1:p.Ile3029Thr
NM_032119.4:c.9086T>C MANE Select	NP_115495.3:p.Ile3029Thr
XM_017009963.2:c.9107T>C	XP_016865452.1:p.Ile3036Thr
XM_017009964.2:c.9104T>C	XP_016865453.1:p.Ile3035Thr
XM_017009965.1:c.9104T>C	XP_016865454.1:p.Ile3035Thr
XM_017009966.2:c.9026T>C	XP_016865455.1:p.Ile3009Thr
XM_017009967.1:c.9011T>C	XP_016865456.1:p.Ile3004Thr
XM_017009968.2:c.9107T>C	XP_016865457.1:p.Ile3036Thr
XM_017009969.2:c.9107T>C	XP_016865458.1:p.Ile3036Thr
XM_017009970.2:c.9107T>C	XP_016865459.1:p.Ile3036Thr
XM_017009971.2:c.9107T>C	XP_016865460.1:p.Ile3036Thr
XM_017009972.1:c.2225T>C	XP_016865461.1:p.Ile742Thr
XM_017009973.1:c.2204T>C	XP_016865462.1:p.Ile735Thr
XM_017009974.2:c.9107T>C	XP_016865463.1:p.Ile3036Thr
NR_003149.2:n.9102T>C