Canonical Allele Identifier: CA360366979

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90627481-C-T
• MyVariant Identifiers: chr5:g.89923298C>T (hg19) ; chr5:g.90627481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627481C>T , CM000667.2:g.90627481C>T	GRCh38
NC_000005.9:g.89923298C>T , CM000667.1:g.89923298C>T	GRCh37
NC_000005.8:g.89959054C>T	NCBI36
NG_007083.1:g.73682C>T
NG_007083.2:g.103138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.943C>T MANE Select	ENSP00000384582.2:p.His315Tyr
ENST00000640083.1:n.648C>T
ENST00000640109.1:n.1039C>T
ENST00000640281.1:n.1002C>T
ENST00000405460.6:c.943C>T	ENSP00000384582.2:p.His315Tyr
NM_032119.3:c.943C>T	NP_115495.3:p.His315Tyr
NR_003149.1:n.1039C>T
XM_011543675.1:c.943C>T	XP_011541977.1:p.His315Tyr
XM_011543676.1:c.943C>T	XP_011541978.1:p.His315Tyr
XM_011543678.1:c.943C>T	XP_011541980.1:p.His315Tyr
XM_011543679.1:c.943C>T	XP_011541981.1:p.His315Tyr
NM_032119.4:c.943C>T MANE Select	NP_115495.3:p.His315Tyr
XM_017009963.2:c.943C>T	XP_016865452.1:p.His315Tyr
XM_017009964.2:c.943C>T	XP_016865453.1:p.His315Tyr
XM_017009965.1:c.940C>T	XP_016865454.1:p.His314Tyr
XM_017009966.2:c.943C>T	XP_016865455.1:p.His315Tyr
XM_017009967.1:c.847C>T	XP_016865456.1:p.His283Tyr
XM_017009968.2:c.943C>T	XP_016865457.1:p.His315Tyr
XM_017009969.2:c.943C>T	XP_016865458.1:p.His315Tyr
XM_017009970.2:c.943C>T	XP_016865459.1:p.His315Tyr
XM_017009971.2:c.943C>T	XP_016865460.1:p.His315Tyr
XM_017009974.2:c.943C>T	XP_016865463.1:p.His315Tyr
NR_003149.2:n.1042C>T