Canonical Allele Identifier: CA445436612

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119395T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823578T>C , CM000667.2:g.90823578T>C	GRCh38
NC_000005.9:g.90119395T>C , CM000667.1:g.90119395T>C	GRCh37
NC_000005.8:g.90155151T>C	NCBI36
NG_007083.1:g.269779T>C
NG_007083.2:g.299235T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16350T>C MANE Select	ENSP00000384582.2:p.Ile5450=
ENST00000425867.3:c.5304T>C	ENSP00000392618.3:p.Ile1768=
ENST00000638510.1:n.3617T>C
ENST00000639431.1:c.265+147369T>C	ENSP00000491057.1:n.265+147369T>C
ENST00000640061.1:n.128+1396T>C
ENST00000640407.1:c.2760T>C	ENSP00000491425.1:p.Ile920=
ENST00000405460.6:c.16350T>C	ENSP00000384582.2:p.Ile5450=
ENST00000425867.2:c.3333T>C	ENSP00000392618.2:p.Ile1111=
NM_032119.3:c.16350T>C	NP_115495.3:p.Ile5450=
NR_003149.1:n.16363T>C
XM_011543675.1:c.16347T>C	XP_011541977.1:p.Ile5449=
XM_011543676.1:c.16269T>C	XP_011541978.1:p.Ile5423=
XM_011543677.1:c.13653T>C	XP_011541979.1:p.Ile4551=
NM_032119.4:c.16350T>C MANE Select	NP_115495.3:p.Ile5450=
XM_017009963.2:c.16371T>C	XP_016865452.1:p.Ile5457=
XM_017009964.2:c.16368T>C	XP_016865453.1:p.Ile5456=
XM_017009965.1:c.16368T>C	XP_016865454.1:p.Ile5456=
XM_017009966.2:c.16290T>C	XP_016865455.1:p.Ile5430=
XM_017009967.1:c.16275T>C	XP_016865456.1:p.Ile5425=
XM_017009968.2:c.16191T>C	XP_016865457.1:p.Ile5397=
XM_017009969.2:c.16371T>C	XP_016865458.1:p.Ile5457=
XM_017009972.1:c.9489T>C	XP_016865461.1:p.Ile3163=
XM_017009973.1:c.9468T>C	XP_016865462.1:p.Ile3156=
NR_003149.2:n.16366T>C