Canonical Allele Identifier: CA445404134

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050930T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755113T>C , CM000667.2:g.90755113T>C	GRCh38
NC_000005.9:g.90050930T>C , CM000667.1:g.90050930T>C	GRCh37
NC_000005.8:g.90086686T>C	NCBI36
NG_007083.1:g.201314T>C
NG_007083.2:g.230770T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11508T>C MANE Select	ENSP00000384582.2:p.Tyr3836=
ENST00000425867.3:c.639T>C	ENSP00000392618.3:p.Tyr213=
ENST00000639431.1:c.265+78904T>C	ENSP00000491057.1:n.265+78904T>C
ENST00000640374.1:n.4652T>C
ENST00000640464.1:n.1927T>C
ENST00000405460.6:c.11508T>C	ENSP00000384582.2:p.Tyr3836=
ENST00000509621.1:c.4205T>C
NM_032119.3:c.11508T>C	NP_115495.3:p.Tyr3836=
NR_003149.1:n.11521T>C
XM_011543675.1:c.11505T>C	XP_011541977.1:p.Tyr3835=
XM_011543676.1:c.11427T>C	XP_011541978.1:p.Tyr3809=
XM_011543677.1:c.8811T>C	XP_011541979.1:p.Tyr2937=
XM_011543678.1:c.11508T>C	XP_011541980.1:p.Tyr3836=
NM_032119.4:c.11508T>C MANE Select	NP_115495.3:p.Tyr3836=
XM_017009963.2:c.11529T>C	XP_016865452.1:p.Tyr3843=
XM_017009964.2:c.11526T>C	XP_016865453.1:p.Tyr3842=
XM_017009965.1:c.11526T>C	XP_016865454.1:p.Tyr3842=
XM_017009966.2:c.11448T>C	XP_016865455.1:p.Tyr3816=
XM_017009967.1:c.11433T>C	XP_016865456.1:p.Tyr3811=
XM_017009968.2:c.11529T>C	XP_016865457.1:p.Tyr3843=
XM_017009969.2:c.11529T>C	XP_016865458.1:p.Tyr3843=
XM_017009970.2:c.11529T>C	XP_016865459.1:p.Tyr3843=
XM_017009971.2:c.11529T>C	XP_016865460.1:p.Tyr3843=
XM_017009972.1:c.4647T>C	XP_016865461.1:p.Tyr1549=
XM_017009973.1:c.4626T>C	XP_016865462.1:p.Tyr1542=
NR_003149.2:n.11524T>C