Canonical Allele Identifier: CA360409180

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041505G>C (hg19) ; chr5:g.90745688G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745688G>C , CM000667.2:g.90745688G>C	GRCh38
NC_000005.9:g.90041505G>C , CM000667.1:g.90041505G>C	GRCh37
NC_000005.8:g.90077261G>C	NCBI36
NG_007083.1:g.191889G>C
NG_007083.2:g.221345G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10867G>C MANE Select	ENSP00000384582.2:p.Val3623Leu
ENST00000639431.1:c.265+69479G>C	ENSP00000491057.1:n.265+69479G>C
ENST00000640374.1:n.4011G>C
ENST00000640464.1:n.1286G>C
ENST00000405460.6:c.10867G>C	ENSP00000384582.2:p.Val3623Leu
ENST00000509621.1:c.3564G>C
NM_032119.3:c.10867G>C	NP_115495.3:p.Val3623Leu
NR_003149.1:n.10880G>C
XM_011543675.1:c.10864G>C	XP_011541977.1:p.Val3622Leu
XM_011543676.1:c.10786G>C	XP_011541978.1:p.Val3596Leu
XM_011543677.1:c.8170G>C	XP_011541979.1:p.Val2724Leu
XM_011543678.1:c.10867G>C	XP_011541980.1:p.Val3623Leu
NM_032119.4:c.10867G>C MANE Select	NP_115495.3:p.Val3623Leu
XM_017009963.2:c.10888G>C	XP_016865452.1:p.Val3630Leu
XM_017009964.2:c.10885G>C	XP_016865453.1:p.Val3629Leu
XM_017009965.1:c.10885G>C	XP_016865454.1:p.Val3629Leu
XM_017009966.2:c.10807G>C	XP_016865455.1:p.Val3603Leu
XM_017009967.1:c.10792G>C	XP_016865456.1:p.Val3598Leu
XM_017009968.2:c.10888G>C	XP_016865457.1:p.Val3630Leu
XM_017009969.2:c.10888G>C	XP_016865458.1:p.Val3630Leu
XM_017009970.2:c.10888G>C	XP_016865459.1:p.Val3630Leu
XM_017009971.2:c.10888G>C	XP_016865460.1:p.Val3630Leu
XM_017009972.1:c.4006G>C	XP_016865461.1:p.Val1336Leu
XM_017009973.1:c.3985G>C	XP_016865462.1:p.Val1329Leu
NR_003149.2:n.10883G>C