Canonical Allele Identifier: CA360426630
Community Standard Title: NM_032119.4(ADGRV1):c.16375C>T (p.Gln5459Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90828950C>T , CM000667.2:g.90828950C>T GRCh38
NC_000005.9:g.90124767C>T , CM000667.1:g.90124767C>T GRCh37
NC_000005.8:g.90160523C>T NCBI36
NG_007083.1:g.275151C>T
NG_007083.2:g.304607C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.16375C>T MANE Select NP_115495.3:p.Gln5459Ter
ENST00000405460.9:c.16375C>T MANE Select ENSP00000384582.2:p.Gln5459Ter
NM_032119.3:c.16375C>T NP_115495.3:p.Gln5459Ter
NR_003149.1:n.16388C>T
NR_003149.2:n.16391C>T
ENST00000405460.6:c.16375C>T ENSP00000384582.2:p.Gln5459Ter
ENST00000425867.2:c.3358C>T ENSP00000392618.2:p.Gln1120Ter
ENST00000425867.3:c.5329C>T ENSP00000392618.3:p.Gln1777Ter
ENST00000638510.1:n.3642C>T
ENST00000639431.1:c.265+152741C>T ENSP00000491057.1:n.265+152741C>T
ENST00000640061.1:n.128+6768C>T
ENST00000640407.1:c.2824C>T ENSP00000491425.1:n.2824C>T
XM_011543675.1:c.16372C>T XP_011541977.1:p.Gln5458Ter
XM_011543676.1:c.16294C>T XP_011541978.1:p.Gln5432Ter
XM_011543677.1:c.13678C>T XP_011541979.1:p.Gln4560Ter
XM_017009963.2:c.16396C>T XP_016865452.1:p.Gln5466Ter
XM_017009964.2:c.16393C>T XP_016865453.1:p.Gln5465Ter
XM_017009965.1:c.16393C>T XP_016865454.1:p.Gln5465Ter
XM_017009966.2:c.16315C>T XP_016865455.1:p.Gln5439Ter
XM_017009967.1:c.16300C>T XP_016865456.1:p.Gln5434Ter
XM_017009968.2:c.16216C>T XP_016865457.1:p.Gln5406Ter
XM_017009969.2:c.16396C>T XP_016865458.1:p.Gln5466Ter
XM_017009972.1:c.9514C>T XP_016865461.1:p.Gln3172Ter
XM_017009973.1:c.9493C>T XP_016865462.1:p.Gln3165Ter