Canonical Allele Identifier: CA2767420613
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692875_90692876insAG , CM000667.2:g.90692875_90692876insAG GRCh38
NC_000005.9:g.89988692_89988693insAG , CM000667.1:g.89988692_89988693insAG GRCh37
NC_000005.8:g.90024448_90024449insAG NCBI36
NG_007083.1:g.139076_139077insAG
NG_007083.2:g.168532_168533insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+89_7133+90insAG MANE Select ENSP00000384582.2:n.7133+89_7133+90insAG
ENST00000639431.1:c.265+16666_265+16667insAG ENSP00000491057.1:n.265+16666_265+16667insAG
ENST00000639473.1:n.2592+89_2592+90insAG
ENST00000640012.1:c.940+89_940+90insAG
ENST00000640374.1:n.277+89_277+90insAG
ENST00000640403.1:c.4424+89_4424+90insAG ENSP00000492531.1:n.4424+89_4424+90insAG
ENST00000640779.1:c.1862+89_1862+90insAG
ENST00000405460.6:c.7133+89_7133+90insAG ENSP00000384582.2:n.7133+89_7133+90insAG
NM_032119.3:c.7133+89_7133+90insAG NP_115495.3:n.7133+89_7133+90insAG
NR_003149.1:n.7146+89_7146+90insAG
XM_011543675.1:c.7130+89_7130+90insAG XP_011541977.1:n.7130+89_7130+90insAG
XM_011543676.1:c.7052+89_7052+90insAG XP_011541978.1:n.7052+89_7052+90insAG
XM_011543677.1:c.4436+89_4436+90insAG XP_011541979.1:n.4436+89_4436+90insAG
XM_011543678.1:c.7133+89_7133+90insAG XP_011541980.1:n.7133+89_7133+90insAG
XM_011543679.1:c.7133+89_7133+90insAG XP_011541981.1:n.7133+89_7133+90insAG
NM_032119.4:c.7133+89_7133+90insAG MANE Select NP_115495.3:n.7133+89_7133+90insAG
XM_017009963.2:c.7133+89_7133+90insAG XP_016865452.1:n.7133+89_7133+90insAG
XM_017009964.2:c.7130+89_7130+90insAG XP_016865453.1:n.7130+89_7130+90insAG
XM_017009965.1:c.7130+89_7130+90insAG XP_016865454.1:n.7130+89_7130+90insAG
XM_017009966.2:c.7052+89_7052+90insAG XP_016865455.1:n.7052+89_7052+90insAG
XM_017009967.1:c.7037+89_7037+90insAG XP_016865456.1:n.7037+89_7037+90insAG
XM_017009968.2:c.7133+89_7133+90insAG XP_016865457.1:n.7133+89_7133+90insAG
XM_017009969.2:c.7133+89_7133+90insAG XP_016865458.1:n.7133+89_7133+90insAG
XM_017009970.2:c.7133+89_7133+90insAG XP_016865459.1:n.7133+89_7133+90insAG
XM_017009971.2:c.7133+89_7133+90insAG XP_016865460.1:n.7133+89_7133+90insAG
XM_017009972.1:c.251+89_251+90insAG XP_016865461.1:n.251+89_251+90insAG
XM_017009973.1:c.251+89_251+90insAG XP_016865462.1:n.251+89_251+90insAG
XM_017009974.2:c.7133+89_7133+90insAG XP_016865463.1:n.7133+89_7133+90insAG
NR_003149.2:n.7149+89_7149+90insAG