Canonical Allele Identifier: CA360403194

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021381A>T (hg19) ; chr5:g.90725564A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725564A>T , CM000667.2:g.90725564A>T	GRCh38
NC_000005.9:g.90021381A>T , CM000667.1:g.90021381A>T	GRCh37
NC_000005.8:g.90057137A>T	NCBI36
NG_007083.1:g.171765A>T
NG_007083.2:g.201221A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10069A>T MANE Select	ENSP00000384582.2:p.Ile3357Phe
ENST00000639431.1:c.265+49355A>T	ENSP00000491057.1:n.265+49355A>T
ENST00000640374.1:n.3213A>T
ENST00000640464.1:n.488A>T
ENST00000405460.6:c.10069A>T	ENSP00000384582.2:p.Ile3357Phe
ENST00000509621.1:c.2766A>T
NM_032119.3:c.10069A>T	NP_115495.3:p.Ile3357Phe
NR_003149.1:n.10082A>T
XM_011543675.1:c.10066A>T	XP_011541977.1:p.Ile3356Phe
XM_011543676.1:c.9988A>T	XP_011541978.1:p.Ile3330Phe
XM_011543677.1:c.7372A>T	XP_011541979.1:p.Ile2458Phe
XM_011543678.1:c.10069A>T	XP_011541980.1:p.Ile3357Phe
XM_011543679.1:c.10069A>T	XP_011541981.1:p.Ile3357Phe
XR_948560.1:n.272-9755T>A
NM_032119.4:c.10069A>T MANE Select	NP_115495.3:p.Ile3357Phe
XM_017009963.2:c.10090A>T	XP_016865452.1:p.Ile3364Phe
XM_017009964.2:c.10087A>T	XP_016865453.1:p.Ile3363Phe
XM_017009965.1:c.10087A>T	XP_016865454.1:p.Ile3363Phe
XM_017009966.2:c.10009A>T	XP_016865455.1:p.Ile3337Phe
XM_017009967.1:c.9994A>T	XP_016865456.1:p.Ile3332Phe
XM_017009968.2:c.10090A>T	XP_016865457.1:p.Ile3364Phe
XM_017009969.2:c.10090A>T	XP_016865458.1:p.Ile3364Phe
XM_017009970.2:c.10090A>T	XP_016865459.1:p.Ile3364Phe
XM_017009971.2:c.10090A>T	XP_016865460.1:p.Ile3364Phe
XM_017009972.1:c.3208A>T	XP_016865461.1:p.Ile1070Phe
XM_017009973.1:c.3187A>T	XP_016865462.1:p.Ile1063Phe
XM_017009974.2:c.10090A>T	XP_016865463.1:p.Ile3364Phe
XR_001742802.1:n.2523-9755T>A
NR_003149.2:n.10085A>T