Canonical Allele Identifier: CA3342404
Community Standard Title: NM_032119.4(ADGRV1):c.17613G>A (p.Gln5871=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90855759G>A , CM000667.2:g.90855759G>A GRCh38
NC_000005.9:g.90151576G>A , CM000667.1:g.90151576G>A GRCh37
NC_000005.8:g.90187332G>A NCBI36
NG_007083.1:g.301960G>A
NG_007083.2:g.331416G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17613G>A MANE Select NP_115495.3:p.Gln5871=
ENST00000405460.9:c.17613G>A MANE Select ENSP00000384582.2:p.Gln5871=
NM_032119.3:c.17613G>A NP_115495.3:p.Gln5871=
NR_003149.1:n.17626G>A
NR_003149.2:n.17629G>A
ENST00000405460.6:c.17613G>A ENSP00000384582.2:p.Gln5871=
ENST00000425867.2:c.4596G>A ENSP00000392618.2:p.Gln1532=
ENST00000425867.3:c.6567G>A ENSP00000392618.3:p.Gln2189=
ENST00000503852.1:n.161G>A
ENST00000638510.1:n.4880G>A
ENST00000638990.1:c.825G>A
ENST00000639431.1:c.266-129585G>A ENSP00000491057.1:n.266-129585G>A
ENST00000640407.1:c.4062G>A ENSP00000491425.1:n.4062G>A
XM_011543675.1:c.17610G>A XP_011541977.1:p.Gln5870=
XM_011543676.1:c.17532G>A XP_011541978.1:p.Gln5844=
XM_011543677.1:c.14916G>A XP_011541979.1:p.Gln4972=
XM_017009963.2:c.17634G>A XP_016865452.1:p.Gln5878=
XM_017009964.2:c.17631G>A XP_016865453.1:p.Gln5877=
XM_017009965.1:c.17631G>A XP_016865454.1:p.Gln5877=
XM_017009966.2:c.17553G>A XP_016865455.1:p.Gln5851=
XM_017009967.1:c.17538G>A XP_016865456.1:p.Gln5846=
XM_017009968.2:c.17454G>A XP_016865457.1:p.Gln5818=
XM_017009969.2:c.17634G>A XP_016865458.1:p.Gln5878=
XM_017009972.1:c.10752G>A XP_016865461.1:p.Gln3584=
XM_017009973.1:c.10731G>A XP_016865462.1:p.Gln3577=