Canonical Allele Identifier: CA3342116
Community Standard Title: NM_032119.4(ADGRV1):c.16325G>A (p.Gly5442Asp)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823553G>A , CM000667.2:g.90823553G>A GRCh38
NC_000005.9:g.90119370G>A , CM000667.1:g.90119370G>A GRCh37
NC_000005.8:g.90155126G>A NCBI36
NG_007083.1:g.269754G>A
NG_007083.2:g.299210G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.16325G>A MANE Select NP_115495.3:p.Gly5442Asp
ENST00000405460.9:c.16325G>A MANE Select ENSP00000384582.2:p.Gly5442Asp
NM_032119.3:c.16325G>A NP_115495.3:p.Gly5442Asp
NR_003149.1:n.16338G>A
NR_003149.2:n.16341G>A
ENST00000405460.6:c.16325G>A ENSP00000384582.2:p.Gly5442Asp
ENST00000425867.2:c.3308G>A ENSP00000392618.2:p.Gly1103Asp
ENST00000425867.3:c.5279G>A ENSP00000392618.3:p.Gly1760Asp
ENST00000638510.1:n.3592G>A
ENST00000639431.1:c.265+147344G>A ENSP00000491057.1:n.265+147344G>A
ENST00000640061.1:n.128+1371G>A
ENST00000640407.1:c.2735G>A ENSP00000491425.1:p.Gly912Asp
XM_011543675.1:c.16322G>A XP_011541977.1:p.Gly5441Asp
XM_011543676.1:c.16244G>A XP_011541978.1:p.Gly5415Asp
XM_011543677.1:c.13628G>A XP_011541979.1:p.Gly4543Asp
XM_017009963.2:c.16346G>A XP_016865452.1:p.Gly5449Asp
XM_017009964.2:c.16343G>A XP_016865453.1:p.Gly5448Asp
XM_017009965.1:c.16343G>A XP_016865454.1:p.Gly5448Asp
XM_017009966.2:c.16265G>A XP_016865455.1:p.Gly5422Asp
XM_017009967.1:c.16250G>A XP_016865456.1:p.Gly5417Asp
XM_017009968.2:c.16166G>A XP_016865457.1:p.Gly5389Asp
XM_017009969.2:c.16346G>A XP_016865458.1:p.Gly5449Asp
XM_017009972.1:c.9464G>A XP_016865461.1:p.Gly3155Asp
XM_017009973.1:c.9443G>A XP_016865462.1:p.Gly3148Asp