Canonical Allele Identifier: CA445436519

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823473-A-G
• MyVariant Identifiers: chr5:g.90119290A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823473A>G , CM000667.2:g.90823473A>G	GRCh38
NC_000005.9:g.90119290A>G , CM000667.1:g.90119290A>G	GRCh37
NC_000005.8:g.90155046A>G	NCBI36
NG_007083.1:g.269674A>G
NG_007083.2:g.299130A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16245A>G MANE Select	ENSP00000384582.2:p.Thr5415=
ENST00000425867.3:c.5199A>G	ENSP00000392618.3:p.Thr1733=
ENST00000638510.1:n.3512A>G
ENST00000639431.1:c.265+147264A>G	ENSP00000491057.1:n.265+147264A>G
ENST00000640061.1:n.128+1291A>G
ENST00000640407.1:c.2655A>G	ENSP00000491425.1:p.Thr885=
ENST00000405460.6:c.16245A>G	ENSP00000384582.2:p.Thr5415=
ENST00000425867.2:c.3228A>G	ENSP00000392618.2:p.Thr1076=
NM_032119.3:c.16245A>G	NP_115495.3:p.Thr5415=
NR_003149.1:n.16258A>G
XM_011543675.1:c.16242A>G	XP_011541977.1:p.Thr5414=
XM_011543676.1:c.16164A>G	XP_011541978.1:p.Thr5388=
XM_011543677.1:c.13548A>G	XP_011541979.1:p.Thr4516=
NM_032119.4:c.16245A>G MANE Select	NP_115495.3:p.Thr5415=
XM_017009963.2:c.16266A>G	XP_016865452.1:p.Thr5422=
XM_017009964.2:c.16263A>G	XP_016865453.1:p.Thr5421=
XM_017009965.1:c.16263A>G	XP_016865454.1:p.Thr5421=
XM_017009966.2:c.16185A>G	XP_016865455.1:p.Thr5395=
XM_017009967.1:c.16170A>G	XP_016865456.1:p.Thr5390=
XM_017009968.2:c.16086A>G	XP_016865457.1:p.Thr5362=
XM_017009969.2:c.16266A>G	XP_016865458.1:p.Thr5422=
XM_017009972.1:c.9384A>G	XP_016865461.1:p.Thr3128=
XM_017009973.1:c.9363A>G	XP_016865462.1:p.Thr3121=
NR_003149.2:n.16261A>G