Canonical Allele Identifier: CA360397820

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012542T>G (hg19) ; chr5:g.90716725T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716725T>G , CM000667.2:g.90716725T>G	GRCh38
NC_000005.9:g.90012542T>G , CM000667.1:g.90012542T>G	GRCh37
NC_000005.8:g.90048298T>G	NCBI36
NG_007083.1:g.162926T>G
NG_007083.2:g.192382T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9443T>G MANE Select	ENSP00000384582.2:p.Phe3148Cys
ENST00000639431.1:c.265+40516T>G	ENSP00000491057.1:n.265+40516T>G
ENST00000639473.1:n.4902T>G
ENST00000640374.1:n.2587T>G
ENST00000640779.1:c.4172T>G
ENST00000405460.6:c.9443T>G	ENSP00000384582.2:p.Phe3148Cys
ENST00000509621.1:c.2140T>G
NM_032119.3:c.9443T>G	NP_115495.3:p.Phe3148Cys
NR_003149.1:n.9456T>G
XM_011543675.1:c.9440T>G	XP_011541977.1:p.Phe3147Cys
XM_011543676.1:c.9362T>G	XP_011541978.1:p.Phe3121Cys
XM_011543677.1:c.6746T>G	XP_011541979.1:p.Phe2249Cys
XM_011543678.1:c.9443T>G	XP_011541980.1:p.Phe3148Cys
XM_011543679.1:c.9443T>G	XP_011541981.1:p.Phe3148Cys
XR_948560.1:n.272-916A>C
NM_032119.4:c.9443T>G MANE Select	NP_115495.3:p.Phe3148Cys
XM_017009963.2:c.9464T>G	XP_016865452.1:p.Phe3155Cys
XM_017009964.2:c.9461T>G	XP_016865453.1:p.Phe3154Cys
XM_017009965.1:c.9461T>G	XP_016865454.1:p.Phe3154Cys
XM_017009966.2:c.9383T>G	XP_016865455.1:p.Phe3128Cys
XM_017009967.1:c.9368T>G	XP_016865456.1:p.Phe3123Cys
XM_017009968.2:c.9464T>G	XP_016865457.1:p.Phe3155Cys
XM_017009969.2:c.9464T>G	XP_016865458.1:p.Phe3155Cys
XM_017009970.2:c.9464T>G	XP_016865459.1:p.Phe3155Cys
XM_017009971.2:c.9464T>G	XP_016865460.1:p.Phe3155Cys
XM_017009972.1:c.2582T>G	XP_016865461.1:p.Phe861Cys
XM_017009973.1:c.2561T>G	XP_016865462.1:p.Phe854Cys
XM_017009974.2:c.9464T>G	XP_016865463.1:p.Phe3155Cys
XR_001742802.1:n.2523-916A>C
NR_003149.2:n.9459T>G