Canonical Allele Identifier: CA360403238

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021400T>C (hg19) ; chr5:g.90725583T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725583T>C , CM000667.2:g.90725583T>C	GRCh38
NC_000005.9:g.90021400T>C , CM000667.1:g.90021400T>C	GRCh37
NC_000005.8:g.90057156T>C	NCBI36
NG_007083.1:g.171784T>C
NG_007083.2:g.201240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10088T>C MANE Select	ENSP00000384582.2:p.Val3363Ala
ENST00000639431.1:c.265+49374T>C	ENSP00000491057.1:n.265+49374T>C
ENST00000640374.1:n.3232T>C
ENST00000640464.1:n.507T>C
ENST00000405460.6:c.10088T>C	ENSP00000384582.2:p.Val3363Ala
ENST00000509621.1:c.2785T>C
NM_032119.3:c.10088T>C	NP_115495.3:p.Val3363Ala
NR_003149.1:n.10101T>C
XM_011543675.1:c.10085T>C	XP_011541977.1:p.Val3362Ala
XM_011543676.1:c.10007T>C	XP_011541978.1:p.Val3336Ala
XM_011543677.1:c.7391T>C	XP_011541979.1:p.Val2464Ala
XM_011543678.1:c.10088T>C	XP_011541980.1:p.Val3363Ala
XM_011543679.1:c.10088T>C	XP_011541981.1:p.Val3363Ala
XR_948560.1:n.272-9774A>G
NM_032119.4:c.10088T>C MANE Select	NP_115495.3:p.Val3363Ala
XM_017009963.2:c.10109T>C	XP_016865452.1:p.Val3370Ala
XM_017009964.2:c.10106T>C	XP_016865453.1:p.Val3369Ala
XM_017009965.1:c.10106T>C	XP_016865454.1:p.Val3369Ala
XM_017009966.2:c.10028T>C	XP_016865455.1:p.Val3343Ala
XM_017009967.1:c.10013T>C	XP_016865456.1:p.Val3338Ala
XM_017009968.2:c.10109T>C	XP_016865457.1:p.Val3370Ala
XM_017009969.2:c.10109T>C	XP_016865458.1:p.Val3370Ala
XM_017009970.2:c.10109T>C	XP_016865459.1:p.Val3370Ala
XM_017009971.2:c.10109T>C	XP_016865460.1:p.Val3370Ala
XM_017009972.1:c.3227T>C	XP_016865461.1:p.Val1076Ala
XM_017009973.1:c.3206T>C	XP_016865462.1:p.Val1069Ala
XM_017009974.2:c.10109T>C	XP_016865463.1:p.Val3370Ala
XR_001742802.1:n.2523-9774A>G
NR_003149.2:n.10104T>C