Canonical Allele Identifier: CA3338652
Community Standard Title: NM_032119.4(ADGRV1):c.1239-1G>T
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90628561G>T , CM000667.2:g.90628561G>T GRCh38
NC_000005.9:g.89924378G>T , CM000667.1:g.89924378G>T GRCh37
NC_000005.8:g.89960134G>T NCBI36
NG_007083.1:g.74762G>T
NG_007083.2:g.104218G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.1239-1G>T MANE Select NP_115495.3:n.1239-1G>T
ENST00000405460.9:c.1239-1G>T MANE Select ENSP00000384582.2:n.1239-1G>T
NM_032119.3:c.1239-1G>T NP_115495.3:n.1239-1G>T
NR_003149.1:n.1335-1G>T
NR_003149.2:n.1338-1G>T
ENST00000405460.6:c.1239-1G>T ENSP00000384582.2:n.1239-1G>T
ENST00000504142.1:c.3G>T
ENST00000504142.2:n.5-1G>T
ENST00000640083.1:n.944-1G>T
ENST00000640109.1:n.1335-1G>T
XM_011543675.1:c.1239-1G>T XP_011541977.1:n.1239-1G>T
XM_011543676.1:c.1239-1G>T XP_011541978.1:n.1239-1G>T
XM_011543678.1:c.1239-1G>T XP_011541980.1:n.1239-1G>T
XM_011543679.1:c.1239-1G>T XP_011541981.1:n.1239-1G>T
XM_017009963.2:c.1239-1G>T XP_016865452.1:n.1239-1G>T
XM_017009964.2:c.1239-1G>T XP_016865453.1:n.1239-1G>T
XM_017009965.1:c.1236-1G>T XP_016865454.1:n.1236-1G>T
XM_017009966.2:c.1239-1G>T XP_016865455.1:n.1239-1G>T
XM_017009967.1:c.1143-1G>T XP_016865456.1:n.1143-1G>T
XM_017009968.2:c.1239-1G>T XP_016865457.1:n.1239-1G>T
XM_017009969.2:c.1239-1G>T XP_016865458.1:n.1239-1G>T
XM_017009970.2:c.1239-1G>T XP_016865459.1:n.1239-1G>T
XM_017009971.2:c.1239-1G>T XP_016865460.1:n.1239-1G>T
XM_017009974.2:c.1239-1G>T XP_016865463.1:n.1239-1G>T