Canonical Allele Identifier: CA3339060
Community Standard Title: NM_032119.4(ADGRV1):c.2923A>G (p.Thr975Ala)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90645992A>G , CM000667.2:g.90645992A>G GRCh38
NC_000005.9:g.89941809A>G , CM000667.1:g.89941809A>G GRCh37
NC_000005.8:g.89977565A>G NCBI36
NG_007083.1:g.92193A>G
NG_007083.2:g.121649A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.2923A>G MANE Select NP_115495.3:p.Thr975Ala
ENST00000405460.9:c.2923A>G MANE Select ENSP00000384582.2:p.Thr975Ala
NM_032119.3:c.2923A>G NP_115495.3:p.Thr975Ala
NR_003149.1:n.3019A>G
NR_003149.2:n.3022A>G
ENST00000405460.6:c.2923A>G ENSP00000384582.2:p.Thr975Ala
ENST00000504142.1:c.1688A>G
ENST00000504142.2:n.1689A>G
ENST00000639676.1:n.521A>G
ENST00000640403.1:c.226A>G ENSP00000492531.1:p.Thr76Ala
XM_011543675.1:c.2923A>G XP_011541977.1:p.Thr975Ala
XM_011543676.1:c.2923A>G XP_011541978.1:p.Thr975Ala
XM_011543677.1:c.226A>G XP_011541979.1:p.Thr76Ala
XM_011543678.1:c.2923A>G XP_011541980.1:p.Thr975Ala
XM_011543679.1:c.2923A>G XP_011541981.1:p.Thr975Ala
XM_017009963.2:c.2923A>G XP_016865452.1:p.Thr975Ala
XM_017009964.2:c.2923A>G XP_016865453.1:p.Thr975Ala
XM_017009965.1:c.2920A>G XP_016865454.1:p.Thr974Ala
XM_017009966.2:c.2923A>G XP_016865455.1:p.Thr975Ala
XM_017009967.1:c.2827A>G XP_016865456.1:p.Thr943Ala
XM_017009968.2:c.2923A>G XP_016865457.1:p.Thr975Ala
XM_017009969.2:c.2923A>G XP_016865458.1:p.Thr975Ala
XM_017009970.2:c.2923A>G XP_016865459.1:p.Thr975Ala
XM_017009971.2:c.2923A>G XP_016865460.1:p.Thr975Ala
XM_017009974.2:c.2923A>G XP_016865463.1:p.Thr975Ala