Canonical Allele Identifier: CA445412067

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712400-T-C
• MyVariant Identifiers: chr5:g.90008217T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712400T>C , CM000667.2:g.90712400T>C	GRCh38
NC_000005.9:g.90008217T>C , CM000667.1:g.90008217T>C	GRCh37
NC_000005.8:g.90043973T>C	NCBI36
NG_007083.1:g.158601T>C
NG_007083.2:g.188057T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9156T>C MANE Select	ENSP00000384582.2:p.Pro3052=
ENST00000639431.1:c.265+36191T>C	ENSP00000491057.1:n.265+36191T>C
ENST00000639473.1:n.4615T>C
ENST00000640012.1:c.2963T>C
ENST00000640374.1:n.2300T>C
ENST00000640779.1:c.3885T>C
ENST00000405460.6:c.9156T>C	ENSP00000384582.2:p.Pro3052=
ENST00000509621.1:c.1853T>C
NM_032119.3:c.9156T>C	NP_115495.3:p.Pro3052=
NR_003149.1:n.9169T>C
XM_011543675.1:c.9153T>C	XP_011541977.1:p.Pro3051=
XM_011543676.1:c.9075T>C	XP_011541978.1:p.Pro3025=
XM_011543677.1:c.6459T>C	XP_011541979.1:p.Pro2153=
XM_011543678.1:c.9156T>C	XP_011541980.1:p.Pro3052=
XM_011543679.1:c.9156T>C	XP_011541981.1:p.Pro3052=
XR_948560.1:n.446A>G
NM_032119.4:c.9156T>C MANE Select	NP_115495.3:p.Pro3052=
XM_017009963.2:c.9177T>C	XP_016865452.1:p.Pro3059=
XM_017009964.2:c.9174T>C	XP_016865453.1:p.Pro3058=
XM_017009965.1:c.9174T>C	XP_016865454.1:p.Pro3058=
XM_017009966.2:c.9096T>C	XP_016865455.1:p.Pro3032=
XM_017009967.1:c.9081T>C	XP_016865456.1:p.Pro3027=
XM_017009968.2:c.9177T>C	XP_016865457.1:p.Pro3059=
XM_017009969.2:c.9177T>C	XP_016865458.1:p.Pro3059=
XM_017009970.2:c.9177T>C	XP_016865459.1:p.Pro3059=
XM_017009971.2:c.9177T>C	XP_016865460.1:p.Pro3059=
XM_017009972.1:c.2295T>C	XP_016865461.1:p.Pro765=
XM_017009973.1:c.2274T>C	XP_016865462.1:p.Pro758=
XM_017009974.2:c.9177T>C	XP_016865463.1:p.Pro3059=
NR_003149.2:n.9172T>C