Canonical Allele Identifier: CA360403190

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021379T>G (hg19) ; chr5:g.90725562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725562T>G , CM000667.2:g.90725562T>G	GRCh38
NC_000005.9:g.90021379T>G , CM000667.1:g.90021379T>G	GRCh37
NC_000005.8:g.90057135T>G	NCBI36
NG_007083.1:g.171763T>G
NG_007083.2:g.201219T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10067T>G MANE Select	ENSP00000384582.2:p.Ile3356Ser
ENST00000639431.1:c.265+49353T>G	ENSP00000491057.1:n.265+49353T>G
ENST00000640374.1:n.3211T>G
ENST00000640464.1:n.486T>G
ENST00000405460.6:c.10067T>G	ENSP00000384582.2:p.Ile3356Ser
ENST00000509621.1:c.2764T>G
NM_032119.3:c.10067T>G	NP_115495.3:p.Ile3356Ser
NR_003149.1:n.10080T>G
XM_011543675.1:c.10064T>G	XP_011541977.1:p.Ile3355Ser
XM_011543676.1:c.9986T>G	XP_011541978.1:p.Ile3329Ser
XM_011543677.1:c.7370T>G	XP_011541979.1:p.Ile2457Ser
XM_011543678.1:c.10067T>G	XP_011541980.1:p.Ile3356Ser
XM_011543679.1:c.10067T>G	XP_011541981.1:p.Ile3356Ser
XR_948560.1:n.272-9753A>C
NM_032119.4:c.10067T>G MANE Select	NP_115495.3:p.Ile3356Ser
XM_017009963.2:c.10088T>G	XP_016865452.1:p.Ile3363Ser
XM_017009964.2:c.10085T>G	XP_016865453.1:p.Ile3362Ser
XM_017009965.1:c.10085T>G	XP_016865454.1:p.Ile3362Ser
XM_017009966.2:c.10007T>G	XP_016865455.1:p.Ile3336Ser
XM_017009967.1:c.9992T>G	XP_016865456.1:p.Ile3331Ser
XM_017009968.2:c.10088T>G	XP_016865457.1:p.Ile3363Ser
XM_017009969.2:c.10088T>G	XP_016865458.1:p.Ile3363Ser
XM_017009970.2:c.10088T>G	XP_016865459.1:p.Ile3363Ser
XM_017009971.2:c.10088T>G	XP_016865460.1:p.Ile3363Ser
XM_017009972.1:c.3206T>G	XP_016865461.1:p.Ile1069Ser
XM_017009973.1:c.3185T>G	XP_016865462.1:p.Ile1062Ser
XM_017009974.2:c.10088T>G	XP_016865463.1:p.Ile3363Ser
XR_001742802.1:n.2523-9753A>C
NR_003149.2:n.10083T>G