Canonical Allele Identifier: CA360403217

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021391G>C (hg19) ; chr5:g.90725574G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725574G>C , CM000667.2:g.90725574G>C	GRCh38
NC_000005.9:g.90021391G>C , CM000667.1:g.90021391G>C	GRCh37
NC_000005.8:g.90057147G>C	NCBI36
NG_007083.1:g.171775G>C
NG_007083.2:g.201231G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10079G>C MANE Select	ENSP00000384582.2:p.Ser3360Thr
ENST00000639431.1:c.265+49365G>C	ENSP00000491057.1:n.265+49365G>C
ENST00000640374.1:n.3223G>C
ENST00000640464.1:n.498G>C
ENST00000405460.6:c.10079G>C	ENSP00000384582.2:p.Ser3360Thr
ENST00000509621.1:c.2776G>C
NM_032119.3:c.10079G>C	NP_115495.3:p.Ser3360Thr
NR_003149.1:n.10092G>C
XM_011543675.1:c.10076G>C	XP_011541977.1:p.Ser3359Thr
XM_011543676.1:c.9998G>C	XP_011541978.1:p.Ser3333Thr
XM_011543677.1:c.7382G>C	XP_011541979.1:p.Ser2461Thr
XM_011543678.1:c.10079G>C	XP_011541980.1:p.Ser3360Thr
XM_011543679.1:c.10079G>C	XP_011541981.1:p.Ser3360Thr
XR_948560.1:n.272-9765C>G
NM_032119.4:c.10079G>C MANE Select	NP_115495.3:p.Ser3360Thr
XM_017009963.2:c.10100G>C	XP_016865452.1:p.Ser3367Thr
XM_017009964.2:c.10097G>C	XP_016865453.1:p.Ser3366Thr
XM_017009965.1:c.10097G>C	XP_016865454.1:p.Ser3366Thr
XM_017009966.2:c.10019G>C	XP_016865455.1:p.Ser3340Thr
XM_017009967.1:c.10004G>C	XP_016865456.1:p.Ser3335Thr
XM_017009968.2:c.10100G>C	XP_016865457.1:p.Ser3367Thr
XM_017009969.2:c.10100G>C	XP_016865458.1:p.Ser3367Thr
XM_017009970.2:c.10100G>C	XP_016865459.1:p.Ser3367Thr
XM_017009971.2:c.10100G>C	XP_016865460.1:p.Ser3367Thr
XM_017009972.1:c.3218G>C	XP_016865461.1:p.Ser1073Thr
XM_017009973.1:c.3197G>C	XP_016865462.1:p.Ser1066Thr
XM_017009974.2:c.10100G>C	XP_016865463.1:p.Ser3367Thr
XR_001742802.1:n.2523-9765C>G
NR_003149.2:n.10095G>C