Canonical Allele Identifier: CA360399085

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085643T>A (hg19) ; chr5:g.90789826T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789826T>A , CM000667.2:g.90789826T>A	GRCh38
NC_000005.9:g.90085643T>A , CM000667.1:g.90085643T>A	GRCh37
NC_000005.8:g.90121399T>A	NCBI36
NG_007083.1:g.236027T>A
NG_007083.2:g.265483T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14018T>A MANE Select	ENSP00000384582.2:p.Val4673Asp
ENST00000425867.3:c.2972T>A	ENSP00000392618.3:p.Val991Asp
ENST00000638510.1:n.1285T>A
ENST00000638975.1:c.647T>A	ENSP00000492630.1:p.Val216Asp
ENST00000639431.1:c.265+113617T>A	ENSP00000491057.1:n.265+113617T>A
ENST00000640407.1:c.428T>A	ENSP00000491425.1:p.Val143Asp
ENST00000405460.6:c.14018T>A	ENSP00000384582.2:p.Val4673Asp
ENST00000425867.2:c.1001T>A	ENSP00000392618.2:p.Val334Asp
NM_032119.3:c.14018T>A	NP_115495.3:p.Val4673Asp
NR_003149.1:n.14031T>A
XM_011543675.1:c.14015T>A	XP_011541977.1:p.Val4672Asp
XM_011543676.1:c.13937T>A	XP_011541978.1:p.Val4646Asp
XM_011543677.1:c.11321T>A	XP_011541979.1:p.Val3774Asp
XM_011543678.1:c.14018T>A	XP_011541980.1:p.Val4673Asp
NM_032119.4:c.14018T>A MANE Select	NP_115495.3:p.Val4673Asp
XM_017009963.2:c.14039T>A	XP_016865452.1:p.Val4680Asp
XM_017009964.2:c.14036T>A	XP_016865453.1:p.Val4679Asp
XM_017009965.1:c.14036T>A	XP_016865454.1:p.Val4679Asp
XM_017009966.2:c.13958T>A	XP_016865455.1:p.Val4653Asp
XM_017009967.1:c.13943T>A	XP_016865456.1:p.Val4648Asp
XM_017009968.2:c.14039T>A	XP_016865457.1:p.Val4680Asp
XM_017009969.2:c.14039T>A	XP_016865458.1:p.Val4680Asp
XM_017009970.2:c.14039T>A	XP_016865459.1:p.Val4680Asp
XM_017009971.2:c.14039T>A	XP_016865460.1:p.Val4680Asp
XM_017009972.1:c.7157T>A	XP_016865461.1:p.Val2386Asp
XM_017009973.1:c.7136T>A	XP_016865462.1:p.Val2379Asp
NR_003149.2:n.14034T>A