Canonical Allele Identifier: CA445436582

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823527-G-C
• MyVariant Identifiers: chr5:g.90119344G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823527G>C , CM000667.2:g.90823527G>C	GRCh38
NC_000005.9:g.90119344G>C , CM000667.1:g.90119344G>C	GRCh37
NC_000005.8:g.90155100G>C	NCBI36
NG_007083.1:g.269728G>C
NG_007083.2:g.299184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16299G>C MANE Select	ENSP00000384582.2:p.Val5433=
ENST00000425867.3:c.5253G>C	ENSP00000392618.3:p.Val1751=
ENST00000638510.1:n.3566G>C
ENST00000639431.1:c.265+147318G>C	ENSP00000491057.1:n.265+147318G>C
ENST00000640061.1:n.128+1345G>C
ENST00000640407.1:c.2709G>C	ENSP00000491425.1:p.Val903=
ENST00000405460.6:c.16299G>C	ENSP00000384582.2:p.Val5433=
ENST00000425867.2:c.3282G>C	ENSP00000392618.2:p.Val1094=
NM_032119.3:c.16299G>C	NP_115495.3:p.Val5433=
NR_003149.1:n.16312G>C
XM_011543675.1:c.16296G>C	XP_011541977.1:p.Val5432=
XM_011543676.1:c.16218G>C	XP_011541978.1:p.Val5406=
XM_011543677.1:c.13602G>C	XP_011541979.1:p.Val4534=
NM_032119.4:c.16299G>C MANE Select	NP_115495.3:p.Val5433=
XM_017009963.2:c.16320G>C	XP_016865452.1:p.Val5440=
XM_017009964.2:c.16317G>C	XP_016865453.1:p.Val5439=
XM_017009965.1:c.16317G>C	XP_016865454.1:p.Val5439=
XM_017009966.2:c.16239G>C	XP_016865455.1:p.Val5413=
XM_017009967.1:c.16224G>C	XP_016865456.1:p.Val5408=
XM_017009968.2:c.16140G>C	XP_016865457.1:p.Val5380=
XM_017009969.2:c.16320G>C	XP_016865458.1:p.Val5440=
XM_017009972.1:c.9438G>C	XP_016865461.1:p.Val3146=
XM_017009973.1:c.9417G>C	XP_016865462.1:p.Val3139=
NR_003149.2:n.16315G>C