Canonical Allele Identifier: CA360403192

Gene: ADGRV1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10069A>C MANE Select	ENSP00000384582.2:p.Ile3357Leu
ENST00000639431.1:c.265+49355A>C	ENSP00000491057.1:n.265+49355A>C
ENST00000640374.1:n.3213A>C
ENST00000640464.1:n.488A>C
ENST00000405460.6:c.10069A>C	ENSP00000384582.2:p.Ile3357Leu
ENST00000509621.1:c.2766A>C
NM_032119.3:c.10069A>C	NP_115495.3:p.Ile3357Leu
NR_003149.1:n.10082A>C
XM_011543675.1:c.10066A>C	XP_011541977.1:p.Ile3356Leu
XM_011543676.1:c.9988A>C	XP_011541978.1:p.Ile3330Leu
XM_011543677.1:c.7372A>C	XP_011541979.1:p.Ile2458Leu
XM_011543678.1:c.10069A>C	XP_011541980.1:p.Ile3357Leu
XM_011543679.1:c.10069A>C	XP_011541981.1:p.Ile3357Leu
XR_948560.1:n.272-9755T>G
NM_032119.4:c.10069A>C MANE Select	NP_115495.3:p.Ile3357Leu
XM_017009963.2:c.10090A>C	XP_016865452.1:p.Ile3364Leu
XM_017009964.2:c.10087A>C	XP_016865453.1:p.Ile3363Leu
XM_017009965.1:c.10087A>C	XP_016865454.1:p.Ile3363Leu
XM_017009966.2:c.10009A>C	XP_016865455.1:p.Ile3337Leu
XM_017009967.1:c.9994A>C	XP_016865456.1:p.Ile3332Leu
XM_017009968.2:c.10090A>C	XP_016865457.1:p.Ile3364Leu
XM_017009969.2:c.10090A>C	XP_016865458.1:p.Ile3364Leu
XM_017009970.2:c.10090A>C	XP_016865459.1:p.Ile3364Leu
XM_017009971.2:c.10090A>C	XP_016865460.1:p.Ile3364Leu
XM_017009972.1:c.3208A>C	XP_016865461.1:p.Ile1070Leu
XM_017009973.1:c.3187A>C	XP_016865462.1:p.Ile1063Leu
XM_017009974.2:c.10090A>C	XP_016865463.1:p.Ile3364Leu
XR_001742802.1:n.2523-9755T>G
NR_003149.2:n.10085A>C