Canonical Allele Identifier: CA360398641
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90789740T>A , CM000667.2:g.90789740T>A GRCh38
NC_000005.9:g.90085557T>A , CM000667.1:g.90085557T>A GRCh37
NC_000005.8:g.90121313T>A NCBI36
NG_007083.1:g.235941T>A
NG_007083.2:g.265397T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.13932T>A MANE Select ENSP00000384582.2:p.Phe4644Leu
ENST00000425867.3:c.2886T>A ENSP00000392618.3:p.Phe962Leu
ENST00000638510.1:n.1199T>A
ENST00000638975.1:c.561T>A ENSP00000492630.1:p.Phe187Leu
ENST00000639431.1:c.265+113531T>A ENSP00000491057.1:n.265+113531T>A
ENST00000640407.1:c.342T>A ENSP00000491425.1:p.Phe114Leu
ENST00000405460.6:c.13932T>A ENSP00000384582.2:p.Phe4644Leu
ENST00000425867.2:c.915T>A ENSP00000392618.2:p.Phe305Leu
NM_032119.3:c.13932T>A NP_115495.3:p.Phe4644Leu
NR_003149.1:n.13945T>A
XM_011543675.1:c.13929T>A XP_011541977.1:p.Phe4643Leu
XM_011543676.1:c.13851T>A XP_011541978.1:p.Phe4617Leu
XM_011543677.1:c.11235T>A XP_011541979.1:p.Phe3745Leu
XM_011543678.1:c.13932T>A XP_011541980.1:p.Phe4644Leu
NM_032119.4:c.13932T>A MANE Select NP_115495.3:p.Phe4644Leu
XM_017009963.2:c.13953T>A XP_016865452.1:p.Phe4651Leu
XM_017009964.2:c.13950T>A XP_016865453.1:p.Phe4650Leu
XM_017009965.1:c.13950T>A XP_016865454.1:p.Phe4650Leu
XM_017009966.2:c.13872T>A XP_016865455.1:p.Phe4624Leu
XM_017009967.1:c.13857T>A XP_016865456.1:p.Phe4619Leu
XM_017009968.2:c.13953T>A XP_016865457.1:p.Phe4651Leu
XM_017009969.2:c.13953T>A XP_016865458.1:p.Phe4651Leu
XM_017009970.2:c.13953T>A XP_016865459.1:p.Phe4651Leu
XM_017009971.2:c.13953T>A XP_016865460.1:p.Phe4651Leu
XM_017009972.1:c.7071T>A XP_016865461.1:p.Phe2357Leu
XM_017009973.1:c.7050T>A XP_016865462.1:p.Phe2350Leu
NR_003149.2:n.13948T>A