Canonical Allele Identifier: CA360410356

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106718T>C (hg19) ; chr5:g.90810901T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810901T>C , CM000667.2:g.90810901T>C	GRCh38
NC_000005.9:g.90106718T>C , CM000667.1:g.90106718T>C	GRCh37
NC_000005.8:g.90142474T>C	NCBI36
NG_007083.1:g.257102T>C
NG_007083.2:g.286558T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15641T>C MANE Select	ENSP00000384582.2:p.Val5214Ala
ENST00000425867.3:c.4595T>C	ENSP00000392618.3:p.Val1532Ala
ENST00000638510.1:n.2908T>C
ENST00000639431.1:c.265+134692T>C	ENSP00000491057.1:n.265+134692T>C
ENST00000640407.1:c.2051T>C	ENSP00000491425.1:p.Val684Ala
ENST00000405460.6:c.15641T>C	ENSP00000384582.2:p.Val5214Ala
ENST00000425867.2:c.2624T>C	ENSP00000392618.2:p.Val875Ala
NM_032119.3:c.15641T>C	NP_115495.3:p.Val5214Ala
NR_003149.1:n.15654T>C
XM_011543675.1:c.15638T>C	XP_011541977.1:p.Val5213Ala
XM_011543676.1:c.15560T>C	XP_011541978.1:p.Val5187Ala
XM_011543677.1:c.12944T>C	XP_011541979.1:p.Val4315Ala
NM_032119.4:c.15641T>C MANE Select	NP_115495.3:p.Val5214Ala
XM_017009963.2:c.15662T>C	XP_016865452.1:p.Val5221Ala
XM_017009964.2:c.15659T>C	XP_016865453.1:p.Val5220Ala
XM_017009965.1:c.15659T>C	XP_016865454.1:p.Val5220Ala
XM_017009966.2:c.15581T>C	XP_016865455.1:p.Val5194Ala
XM_017009967.1:c.15566T>C	XP_016865456.1:p.Val5189Ala
XM_017009968.2:c.15482T>C	XP_016865457.1:p.Val5161Ala
XM_017009969.2:c.15662T>C	XP_016865458.1:p.Val5221Ala
XM_017009972.1:c.8780T>C	XP_016865461.1:p.Val2927Ala
XM_017009973.1:c.8759T>C	XP_016865462.1:p.Val2920Ala
NR_003149.2:n.15657T>C