Canonical Allele Identifier: CA445413854

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012483T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716666T>C , CM000667.2:g.90716666T>C	GRCh38
NC_000005.9:g.90012483T>C , CM000667.1:g.90012483T>C	GRCh37
NC_000005.8:g.90048239T>C	NCBI36
NG_007083.1:g.162867T>C
NG_007083.2:g.192323T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9384T>C MANE Select	ENSP00000384582.2:p.Asn3128=
ENST00000639431.1:c.265+40457T>C	ENSP00000491057.1:n.265+40457T>C
ENST00000639473.1:n.4843T>C
ENST00000640012.1:c.3191T>C
ENST00000640374.1:n.2528T>C
ENST00000640779.1:c.4113T>C
ENST00000405460.6:c.9384T>C	ENSP00000384582.2:p.Asn3128=
ENST00000509621.1:c.2081T>C
NM_032119.3:c.9384T>C	NP_115495.3:p.Asn3128=
NR_003149.1:n.9397T>C
XM_011543675.1:c.9381T>C	XP_011541977.1:p.Asn3127=
XM_011543676.1:c.9303T>C	XP_011541978.1:p.Asn3101=
XM_011543677.1:c.6687T>C	XP_011541979.1:p.Asn2229=
XM_011543678.1:c.9384T>C	XP_011541980.1:p.Asn3128=
XM_011543679.1:c.9384T>C	XP_011541981.1:p.Asn3128=
XR_948560.1:n.272-857A>G
NM_032119.4:c.9384T>C MANE Select	NP_115495.3:p.Asn3128=
XM_017009963.2:c.9405T>C	XP_016865452.1:p.Asn3135=
XM_017009964.2:c.9402T>C	XP_016865453.1:p.Asn3134=
XM_017009965.1:c.9402T>C	XP_016865454.1:p.Asn3134=
XM_017009966.2:c.9324T>C	XP_016865455.1:p.Asn3108=
XM_017009967.1:c.9309T>C	XP_016865456.1:p.Asn3103=
XM_017009968.2:c.9405T>C	XP_016865457.1:p.Asn3135=
XM_017009969.2:c.9405T>C	XP_016865458.1:p.Asn3135=
XM_017009970.2:c.9405T>C	XP_016865459.1:p.Asn3135=
XM_017009971.2:c.9405T>C	XP_016865460.1:p.Asn3135=
XM_017009972.1:c.2523T>C	XP_016865461.1:p.Asn841=
XM_017009973.1:c.2502T>C	XP_016865462.1:p.Asn834=
XM_017009974.2:c.9405T>C	XP_016865463.1:p.Asn3135=
XR_001742802.1:n.2523-857A>G
NR_003149.2:n.9400T>C