Canonical Allele Identifier: CA445413785

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012465A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716648A>C , CM000667.2:g.90716648A>C	GRCh38
NC_000005.9:g.90012465A>C , CM000667.1:g.90012465A>C	GRCh37
NC_000005.8:g.90048221A>C	NCBI36
NG_007083.1:g.162849A>C
NG_007083.2:g.192305A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9366A>C MANE Select	ENSP00000384582.2:p.Thr3122=
ENST00000639431.1:c.265+40439A>C	ENSP00000491057.1:n.265+40439A>C
ENST00000639473.1:n.4825A>C
ENST00000640012.1:c.3173A>C
ENST00000640374.1:n.2510A>C
ENST00000640779.1:c.4095A>C
ENST00000405460.6:c.9366A>C	ENSP00000384582.2:p.Thr3122=
ENST00000509621.1:c.2063A>C
NM_032119.3:c.9366A>C	NP_115495.3:p.Thr3122=
NR_003149.1:n.9379A>C
XM_011543675.1:c.9363A>C	XP_011541977.1:p.Thr3121=
XM_011543676.1:c.9285A>C	XP_011541978.1:p.Thr3095=
XM_011543677.1:c.6669A>C	XP_011541979.1:p.Thr2223=
XM_011543678.1:c.9366A>C	XP_011541980.1:p.Thr3122=
XM_011543679.1:c.9366A>C	XP_011541981.1:p.Thr3122=
XR_948560.1:n.272-839T>G
NM_032119.4:c.9366A>C MANE Select	NP_115495.3:p.Thr3122=
XM_017009963.2:c.9387A>C	XP_016865452.1:p.Thr3129=
XM_017009964.2:c.9384A>C	XP_016865453.1:p.Thr3128=
XM_017009965.1:c.9384A>C	XP_016865454.1:p.Thr3128=
XM_017009966.2:c.9306A>C	XP_016865455.1:p.Thr3102=
XM_017009967.1:c.9291A>C	XP_016865456.1:p.Thr3097=
XM_017009968.2:c.9387A>C	XP_016865457.1:p.Thr3129=
XM_017009969.2:c.9387A>C	XP_016865458.1:p.Thr3129=
XM_017009970.2:c.9387A>C	XP_016865459.1:p.Thr3129=
XM_017009971.2:c.9387A>C	XP_016865460.1:p.Thr3129=
XM_017009972.1:c.2505A>C	XP_016865461.1:p.Thr835=
XM_017009973.1:c.2484A>C	XP_016865462.1:p.Thr828=
XM_017009974.2:c.9387A>C	XP_016865463.1:p.Thr3129=
XR_001742802.1:n.2523-839T>G
NR_003149.2:n.9382A>C