Canonical Allele Identifier: CA360385920

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89913744A>C (hg19) ; chr5:g.90617927A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617927A>C , CM000667.2:g.90617927A>C	GRCh38
NC_000005.9:g.89913744A>C , CM000667.1:g.89913744A>C	GRCh37
NC_000005.8:g.89949500A>C	NCBI36
NG_007083.1:g.64128A>C
NG_007083.2:g.93584A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.331A>C MANE Select	ENSP00000384582.2:p.Thr111Pro
ENST00000638316.1:n.541A>C
ENST00000638638.1:n.738A>C
ENST00000640083.1:n.36A>C
ENST00000640109.1:n.427A>C
ENST00000640281.1:n.390A>C
ENST00000405460.6:c.331A>C	ENSP00000384582.2:p.Thr111Pro
ENST00000508842.5:c.343A>C	ENSP00000425936.1:p.Thr115Pro
NM_032119.3:c.331A>C	NP_115495.3:p.Thr111Pro
NR_003149.1:n.427A>C
XM_011543675.1:c.331A>C	XP_011541977.1:p.Thr111Pro
XM_011543676.1:c.331A>C	XP_011541978.1:p.Thr111Pro
XM_011543678.1:c.331A>C	XP_011541980.1:p.Thr111Pro
XM_011543679.1:c.331A>C	XP_011541981.1:p.Thr111Pro
NM_032119.4:c.331A>C MANE Select	NP_115495.3:p.Thr111Pro
XM_017009963.2:c.331A>C	XP_016865452.1:p.Thr111Pro
XM_017009964.2:c.331A>C	XP_016865453.1:p.Thr111Pro
XM_017009965.1:c.328A>C	XP_016865454.1:p.Thr110Pro
XM_017009966.2:c.331A>C	XP_016865455.1:p.Thr111Pro
XM_017009967.1:c.331A>C	XP_016865456.1:p.Thr111Pro
XM_017009968.2:c.331A>C	XP_016865457.1:p.Thr111Pro
XM_017009969.2:c.331A>C	XP_016865458.1:p.Thr111Pro
XM_017009970.2:c.331A>C	XP_016865459.1:p.Thr111Pro
XM_017009971.2:c.331A>C	XP_016865460.1:p.Thr111Pro
XM_017009974.2:c.331A>C	XP_016865463.1:p.Thr111Pro
NR_003149.2:n.430A>C