Canonical Allele Identifier: CA360397396
Community Standard Title: NM_032119.4(ADGRV1):c.9325C>T (p.Gln3109Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716607C>T , CM000667.2:g.90716607C>T GRCh38
NC_000005.9:g.90012424C>T , CM000667.1:g.90012424C>T GRCh37
NC_000005.8:g.90048180C>T NCBI36
NG_007083.1:g.162808C>T
NG_007083.2:g.192264C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.9325C>T MANE Select NP_115495.3:p.Gln3109Ter
ENST00000405460.9:c.9325C>T MANE Select ENSP00000384582.2:p.Gln3109Ter
NM_032119.3:c.9325C>T NP_115495.3:p.Gln3109Ter
NR_003149.1:n.9338C>T
NR_003149.2:n.9341C>T
ENST00000405460.6:c.9325C>T ENSP00000384582.2:p.Gln3109Ter
ENST00000509621.1:c.2022C>T
ENST00000639431.1:c.265+40398C>T ENSP00000491057.1:n.265+40398C>T
ENST00000639473.1:n.4784C>T
ENST00000640012.1:c.3132C>T
ENST00000640374.1:n.2469C>T
ENST00000640779.1:c.4054C>T
XM_011543675.1:c.9322C>T XP_011541977.1:p.Gln3108Ter
XM_011543676.1:c.9244C>T XP_011541978.1:p.Gln3082Ter
XM_011543677.1:c.6628C>T XP_011541979.1:p.Gln2210Ter
XM_011543678.1:c.9325C>T XP_011541980.1:p.Gln3109Ter
XM_011543679.1:c.9325C>T XP_011541981.1:p.Gln3109Ter
XM_017009963.2:c.9346C>T XP_016865452.1:p.Gln3116Ter
XM_017009964.2:c.9343C>T XP_016865453.1:p.Gln3115Ter
XM_017009965.1:c.9343C>T XP_016865454.1:p.Gln3115Ter
XM_017009966.2:c.9265C>T XP_016865455.1:p.Gln3089Ter
XM_017009967.1:c.9250C>T XP_016865456.1:p.Gln3084Ter
XM_017009968.2:c.9346C>T XP_016865457.1:p.Gln3116Ter
XM_017009969.2:c.9346C>T XP_016865458.1:p.Gln3116Ter
XM_017009970.2:c.9346C>T XP_016865459.1:p.Gln3116Ter
XM_017009971.2:c.9346C>T XP_016865460.1:p.Gln3116Ter
XM_017009972.1:c.2464C>T XP_016865461.1:p.Gln822Ter
XM_017009973.1:c.2443C>T XP_016865462.1:p.Gln815Ter
XM_017009974.2:c.9346C>T XP_016865463.1:p.Gln3116Ter
XR_001742802.1:n.2523-798G>A
XR_948560.1:n.272-798G>A