Canonical Allele Identifier: CA360426638

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90124769G>C (hg19) ; chr5:g.90828952G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90828952G>C , CM000667.2:g.90828952G>C	GRCh38
NC_000005.9:g.90124769G>C , CM000667.1:g.90124769G>C	GRCh37
NC_000005.8:g.90160525G>C	NCBI36
NG_007083.1:g.275153G>C
NG_007083.2:g.304609G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16377G>C MANE Select	ENSP00000384582.2:p.Gln5459His
ENST00000425867.3:c.5331G>C	ENSP00000392618.3:p.Gln1777His
ENST00000638510.1:n.3644G>C
ENST00000639431.1:c.265+152743G>C	ENSP00000491057.1:n.265+152743G>C
ENST00000640061.1:n.128+6770G>C
ENST00000640407.1:c.2826G>C	ENSP00000491425.1:n.2826G>C
ENST00000405460.6:c.16377G>C	ENSP00000384582.2:p.Gln5459His
ENST00000425867.2:c.3360G>C	ENSP00000392618.2:p.Gln1120His
NM_032119.3:c.16377G>C	NP_115495.3:p.Gln5459His
NR_003149.1:n.16390G>C
XM_011543675.1:c.16374G>C	XP_011541977.1:p.Gln5458His
XM_011543676.1:c.16296G>C	XP_011541978.1:p.Gln5432His
XM_011543677.1:c.13680G>C	XP_011541979.1:p.Gln4560His
NM_032119.4:c.16377G>C MANE Select	NP_115495.3:p.Gln5459His
XM_017009963.2:c.16398G>C	XP_016865452.1:p.Gln5466His
XM_017009964.2:c.16395G>C	XP_016865453.1:p.Gln5465His
XM_017009965.1:c.16395G>C	XP_016865454.1:p.Gln5465His
XM_017009966.2:c.16317G>C	XP_016865455.1:p.Gln5439His
XM_017009967.1:c.16302G>C	XP_016865456.1:p.Gln5434His
XM_017009968.2:c.16218G>C	XP_016865457.1:p.Gln5406His
XM_017009969.2:c.16398G>C	XP_016865458.1:p.Gln5466His
XM_017009972.1:c.9516G>C	XP_016865461.1:p.Gln3172His
XM_017009973.1:c.9495G>C	XP_016865462.1:p.Gln3165His
NR_003149.2:n.16393G>C