Canonical Allele Identifier: CA3340727
Community Standard Title: NM_032119.4(ADGRV1):c.10322G>C (p.Gly3441Ala)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90728829G>C , CM000667.2:g.90728829G>C GRCh38
NC_000005.9:g.90024646G>C , CM000667.1:g.90024646G>C GRCh37
NC_000005.8:g.90060402G>C NCBI36
NG_007083.1:g.175030G>C
NG_007083.2:g.204486G>C

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10322G>C MANE Select NP_115495.3:p.Gly3441Ala
ENST00000405460.9:c.10322G>C MANE Select ENSP00000384582.2:p.Gly3441Ala
NM_032119.3:c.10322G>C NP_115495.3:p.Gly3441Ala
NR_003149.1:n.10335G>C
NR_003149.2:n.10338G>C
ENST00000405460.6:c.10322G>C ENSP00000384582.2:p.Gly3441Ala
ENST00000509621.1:c.3019G>C
ENST00000639431.1:c.265+52620G>C ENSP00000491057.1:n.265+52620G>C
ENST00000640374.1:n.3466G>C
ENST00000640464.1:n.741G>C
XM_011543675.1:c.10319G>C XP_011541977.1:p.Gly3440Ala
XM_011543676.1:c.10241G>C XP_011541978.1:p.Gly3414Ala
XM_011543677.1:c.7625G>C XP_011541979.1:p.Gly2542Ala
XM_011543678.1:c.10322G>C XP_011541980.1:p.Gly3441Ala
XM_011543679.1:c.10322G>C XP_011541981.1:p.Gly3441Ala
XM_017009963.2:c.10343G>C XP_016865452.1:p.Gly3448Ala
XM_017009964.2:c.10340G>C XP_016865453.1:p.Gly3447Ala
XM_017009965.1:c.10340G>C XP_016865454.1:p.Gly3447Ala
XM_017009966.2:c.10262G>C XP_016865455.1:p.Gly3421Ala
XM_017009967.1:c.10247G>C XP_016865456.1:p.Gly3416Ala
XM_017009968.2:c.10343G>C XP_016865457.1:p.Gly3448Ala
XM_017009969.2:c.10343G>C XP_016865458.1:p.Gly3448Ala
XM_017009970.2:c.10343G>C XP_016865459.1:p.Gly3448Ala
XM_017009971.2:c.10343G>C XP_016865460.1:p.Gly3448Ala
XM_017009972.1:c.3461G>C XP_016865461.1:p.Gly1154Ala
XM_017009973.1:c.3440G>C XP_016865462.1:p.Gly1147Ala
XM_017009974.2:c.10343G>C XP_016865463.1:p.Gly3448Ala
XR_001742802.1:n.2522+12078C>G
XR_948560.1:n.271+12078C>G