Canonical Allele Identifier: CA360397562

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012470T>C (hg19) ; chr5:g.90716653T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716653T>C , CM000667.2:g.90716653T>C	GRCh38
NC_000005.9:g.90012470T>C , CM000667.1:g.90012470T>C	GRCh37
NC_000005.8:g.90048226T>C	NCBI36
NG_007083.1:g.162854T>C
NG_007083.2:g.192310T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9371T>C MANE Select	ENSP00000384582.2:p.Val3124Ala
ENST00000639431.1:c.265+40444T>C	ENSP00000491057.1:n.265+40444T>C
ENST00000639473.1:n.4830T>C
ENST00000640012.1:c.3178T>C
ENST00000640374.1:n.2515T>C
ENST00000640779.1:c.4100T>C
ENST00000405460.6:c.9371T>C	ENSP00000384582.2:p.Val3124Ala
ENST00000509621.1:c.2068T>C
NM_032119.3:c.9371T>C	NP_115495.3:p.Val3124Ala
NR_003149.1:n.9384T>C
XM_011543675.1:c.9368T>C	XP_011541977.1:p.Val3123Ala
XM_011543676.1:c.9290T>C	XP_011541978.1:p.Val3097Ala
XM_011543677.1:c.6674T>C	XP_011541979.1:p.Val2225Ala
XM_011543678.1:c.9371T>C	XP_011541980.1:p.Val3124Ala
XM_011543679.1:c.9371T>C	XP_011541981.1:p.Val3124Ala
XR_948560.1:n.272-844A>G
NM_032119.4:c.9371T>C MANE Select	NP_115495.3:p.Val3124Ala
XM_017009963.2:c.9392T>C	XP_016865452.1:p.Val3131Ala
XM_017009964.2:c.9389T>C	XP_016865453.1:p.Val3130Ala
XM_017009965.1:c.9389T>C	XP_016865454.1:p.Val3130Ala
XM_017009966.2:c.9311T>C	XP_016865455.1:p.Val3104Ala
XM_017009967.1:c.9296T>C	XP_016865456.1:p.Val3099Ala
XM_017009968.2:c.9392T>C	XP_016865457.1:p.Val3131Ala
XM_017009969.2:c.9392T>C	XP_016865458.1:p.Val3131Ala
XM_017009970.2:c.9392T>C	XP_016865459.1:p.Val3131Ala
XM_017009971.2:c.9392T>C	XP_016865460.1:p.Val3131Ala
XM_017009972.1:c.2510T>C	XP_016865461.1:p.Val837Ala
XM_017009973.1:c.2489T>C	XP_016865462.1:p.Val830Ala
XM_017009974.2:c.9392T>C	XP_016865463.1:p.Val3131Ala
XR_001742802.1:n.2523-844A>G
NR_003149.2:n.9387T>C