Canonical Allele Identifier: CA245868
Community Standard Title: NM_032119.4(ADGRV1):c.10323G>T (p.Gly3441=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90728830G>T , CM000667.2:g.90728830G>T GRCh38
NC_000005.9:g.90024647G>T , CM000667.1:g.90024647G>T GRCh37
NC_000005.8:g.90060403G>T NCBI36
NG_007083.1:g.175031G>T
NG_007083.2:g.204487G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10323G>T MANE Select NP_115495.3:p.Gly3441=
ENST00000405460.9:c.10323G>T MANE Select ENSP00000384582.2:p.Gly3441=
NM_032119.3:c.10323G>T NP_115495.3:p.Gly3441=
NR_003149.1:n.10336G>T
NR_003149.2:n.10339G>T
ENST00000405460.6:c.10323G>T ENSP00000384582.2:p.Gly3441=
ENST00000509621.1:c.3020G>T
ENST00000639431.1:c.265+52621G>T ENSP00000491057.1:n.265+52621G>T
ENST00000640374.1:n.3467G>T
ENST00000640464.1:n.742G>T
XM_011543675.1:c.10320G>T XP_011541977.1:p.Gly3440=
XM_011543676.1:c.10242G>T XP_011541978.1:p.Gly3414=
XM_011543677.1:c.7626G>T XP_011541979.1:p.Gly2542=
XM_011543678.1:c.10323G>T XP_011541980.1:p.Gly3441=
XM_011543679.1:c.10323G>T XP_011541981.1:p.Gly3441=
XM_017009963.2:c.10344G>T XP_016865452.1:p.Gly3448=
XM_017009964.2:c.10341G>T XP_016865453.1:p.Gly3447=
XM_017009965.1:c.10341G>T XP_016865454.1:p.Gly3447=
XM_017009966.2:c.10263G>T XP_016865455.1:p.Gly3421=
XM_017009967.1:c.10248G>T XP_016865456.1:p.Gly3416=
XM_017009968.2:c.10344G>T XP_016865457.1:p.Gly3448=
XM_017009969.2:c.10344G>T XP_016865458.1:p.Gly3448=
XM_017009970.2:c.10344G>T XP_016865459.1:p.Gly3448=
XM_017009971.2:c.10344G>T XP_016865460.1:p.Gly3448=
XM_017009972.1:c.3462G>T XP_016865461.1:p.Gly1154=
XM_017009973.1:c.3441G>T XP_016865462.1:p.Gly1147=
XM_017009974.2:c.10344G>T XP_016865463.1:p.Gly3448=
XR_001742802.1:n.2522+12077C>A
XR_948560.1:n.271+12077C>A