Canonical Allele Identifier: CA360396196

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008141T>C (hg19) ; chr5:g.90712324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712324T>C , CM000667.2:g.90712324T>C	GRCh38
NC_000005.9:g.90008141T>C , CM000667.1:g.90008141T>C	GRCh37
NC_000005.8:g.90043897T>C	NCBI36
NG_007083.1:g.158525T>C
NG_007083.2:g.187981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9080T>C MANE Select	ENSP00000384582.2:p.Val3027Ala
ENST00000639431.1:c.265+36115T>C	ENSP00000491057.1:n.265+36115T>C
ENST00000639473.1:n.4539T>C
ENST00000640012.1:c.2887T>C
ENST00000640374.1:n.2224T>C
ENST00000640779.1:c.3809T>C
ENST00000405460.6:c.9080T>C	ENSP00000384582.2:p.Val3027Ala
ENST00000509621.1:c.1777T>C
NM_032119.3:c.9080T>C	NP_115495.3:p.Val3027Ala
NR_003149.1:n.9093T>C
XM_011543675.1:c.9077T>C	XP_011541977.1:p.Val3026Ala
XM_011543676.1:c.8999T>C	XP_011541978.1:p.Val3000Ala
XM_011543677.1:c.6383T>C	XP_011541979.1:p.Val2128Ala
XM_011543678.1:c.9080T>C	XP_011541980.1:p.Val3027Ala
XM_011543679.1:c.9080T>C	XP_011541981.1:p.Val3027Ala
NM_032119.4:c.9080T>C MANE Select	NP_115495.3:p.Val3027Ala
XM_017009963.2:c.9101T>C	XP_016865452.1:p.Val3034Ala
XM_017009964.2:c.9098T>C	XP_016865453.1:p.Val3033Ala
XM_017009965.1:c.9098T>C	XP_016865454.1:p.Val3033Ala
XM_017009966.2:c.9020T>C	XP_016865455.1:p.Val3007Ala
XM_017009967.1:c.9005T>C	XP_016865456.1:p.Val3002Ala
XM_017009968.2:c.9101T>C	XP_016865457.1:p.Val3034Ala
XM_017009969.2:c.9101T>C	XP_016865458.1:p.Val3034Ala
XM_017009970.2:c.9101T>C	XP_016865459.1:p.Val3034Ala
XM_017009971.2:c.9101T>C	XP_016865460.1:p.Val3034Ala
XM_017009972.1:c.2219T>C	XP_016865461.1:p.Val740Ala
XM_017009973.1:c.2198T>C	XP_016865462.1:p.Val733Ala
XM_017009974.2:c.9101T>C	XP_016865463.1:p.Val3034Ala
NR_003149.2:n.9096T>C