Canonical Allele Identifier: CA3342044
Community Standard Title: NM_032119.4(ADGRV1):c.16079-11C>G
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90815608C>G , CM000667.2:g.90815608C>G GRCh38
NC_000005.9:g.90111425C>G , CM000667.1:g.90111425C>G GRCh37
NC_000005.8:g.90147181C>G NCBI36
NG_007083.1:g.261809C>G
NG_007083.2:g.291265C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.16079-11C>G MANE Select NP_115495.3:n.16079-11C>G
ENST00000405460.9:c.16079-11C>G MANE Select ENSP00000384582.2:n.16079-11C>G
NM_032119.3:c.16079-11C>G NP_115495.3:n.16079-11C>G
NR_003149.1:n.16092-11C>G
NR_003149.2:n.16095-11C>G
ENST00000405460.6:c.16079-11C>G ENSP00000384582.2:n.16079-11C>G
ENST00000425867.2:c.3062-11C>G ENSP00000392618.2:n.3062-11C>G
ENST00000425867.3:c.5033-11C>G ENSP00000392618.3:n.5033-11C>G
ENST00000638510.1:n.3346-11C>G
ENST00000639431.1:c.265+139399C>G ENSP00000491057.1:n.265+139399C>G
ENST00000640407.1:c.2489-11C>G ENSP00000491425.1:n.2489-11C>G
XM_011543675.1:c.16076-11C>G XP_011541977.1:n.16076-11C>G
XM_011543676.1:c.15998-11C>G XP_011541978.1:n.15998-11C>G
XM_011543677.1:c.13382-11C>G XP_011541979.1:n.13382-11C>G
XM_017009963.2:c.16100-11C>G XP_016865452.1:n.16100-11C>G
XM_017009964.2:c.16097-11C>G XP_016865453.1:n.16097-11C>G
XM_017009965.1:c.16097-11C>G XP_016865454.1:n.16097-11C>G
XM_017009966.2:c.16019-11C>G XP_016865455.1:n.16019-11C>G
XM_017009967.1:c.16004-11C>G XP_016865456.1:n.16004-11C>G
XM_017009968.2:c.15920-11C>G XP_016865457.1:n.15920-11C>G
XM_017009969.2:c.16100-11C>G XP_016865458.1:n.16100-11C>G
XM_017009972.1:c.9218-11C>G XP_016865461.1:n.9218-11C>G
XM_017009973.1:c.9197-11C>G XP_016865462.1:n.9197-11C>G