Canonical Allele Identifier: CA360412593
Community Standard Title: NM_032119.4(ADGRV1):c.16147G>T (p.Gly5383Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90815687G>T , CM000667.2:g.90815687G>T GRCh38
NC_000005.9:g.90111504G>T , CM000667.1:g.90111504G>T GRCh37
NC_000005.8:g.90147260G>T NCBI36
NG_007083.1:g.261888G>T
NG_007083.2:g.291344G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.16147G>T MANE Select NP_115495.3:p.Gly5383Ter
ENST00000405460.9:c.16147G>T MANE Select ENSP00000384582.2:p.Gly5383Ter
NM_032119.3:c.16147G>T NP_115495.3:p.Gly5383Ter
NR_003149.1:n.16160G>T
NR_003149.2:n.16163G>T
ENST00000405460.6:c.16147G>T ENSP00000384582.2:p.Gly5383Ter
ENST00000425867.2:c.3130G>T ENSP00000392618.2:p.Gly1044Ter
ENST00000425867.3:c.5101G>T ENSP00000392618.3:p.Gly1701Ter
ENST00000638510.1:n.3414G>T
ENST00000639431.1:c.265+139478G>T ENSP00000491057.1:n.265+139478G>T
ENST00000640407.1:c.2557G>T ENSP00000491425.1:p.Gly853Ter
XM_011543675.1:c.16144G>T XP_011541977.1:p.Gly5382Ter
XM_011543676.1:c.16066G>T XP_011541978.1:p.Gly5356Ter
XM_011543677.1:c.13450G>T XP_011541979.1:p.Gly4484Ter
XM_017009963.2:c.16168G>T XP_016865452.1:p.Gly5390Ter
XM_017009964.2:c.16165G>T XP_016865453.1:p.Gly5389Ter
XM_017009965.1:c.16165G>T XP_016865454.1:p.Gly5389Ter
XM_017009966.2:c.16087G>T XP_016865455.1:p.Gly5363Ter
XM_017009967.1:c.16072G>T XP_016865456.1:p.Gly5358Ter
XM_017009968.2:c.15988G>T XP_016865457.1:p.Gly5330Ter
XM_017009969.2:c.16168G>T XP_016865458.1:p.Gly5390Ter
XM_017009972.1:c.9286G>T XP_016865461.1:p.Gly3096Ter
XM_017009973.1:c.9265G>T XP_016865462.1:p.Gly3089Ter