Canonical Allele Identifier: CA360410380

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106724T>G (hg19) ; chr5:g.90810907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810907T>G , CM000667.2:g.90810907T>G	GRCh38
NC_000005.9:g.90106724T>G , CM000667.1:g.90106724T>G	GRCh37
NC_000005.8:g.90142480T>G	NCBI36
NG_007083.1:g.257108T>G
NG_007083.2:g.286564T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15647T>G MANE Select	ENSP00000384582.2:p.Ile5216Ser
ENST00000425867.3:c.4601T>G	ENSP00000392618.3:p.Ile1534Ser
ENST00000638510.1:n.2914T>G
ENST00000639431.1:c.265+134698T>G	ENSP00000491057.1:n.265+134698T>G
ENST00000640407.1:c.2057T>G	ENSP00000491425.1:p.Ile686Ser
ENST00000405460.6:c.15647T>G	ENSP00000384582.2:p.Ile5216Ser
ENST00000425867.2:c.2630T>G	ENSP00000392618.2:p.Ile877Ser
NM_032119.3:c.15647T>G	NP_115495.3:p.Ile5216Ser
NR_003149.1:n.15660T>G
XM_011543675.1:c.15644T>G	XP_011541977.1:p.Ile5215Ser
XM_011543676.1:c.15566T>G	XP_011541978.1:p.Ile5189Ser
XM_011543677.1:c.12950T>G	XP_011541979.1:p.Ile4317Ser
NM_032119.4:c.15647T>G MANE Select	NP_115495.3:p.Ile5216Ser
XM_017009963.2:c.15668T>G	XP_016865452.1:p.Ile5223Ser
XM_017009964.2:c.15665T>G	XP_016865453.1:p.Ile5222Ser
XM_017009965.1:c.15665T>G	XP_016865454.1:p.Ile5222Ser
XM_017009966.2:c.15587T>G	XP_016865455.1:p.Ile5196Ser
XM_017009967.1:c.15572T>G	XP_016865456.1:p.Ile5191Ser
XM_017009968.2:c.15488T>G	XP_016865457.1:p.Ile5163Ser
XM_017009969.2:c.15668T>G	XP_016865458.1:p.Ile5223Ser
XM_017009972.1:c.8786T>G	XP_016865461.1:p.Ile2929Ser
XM_017009973.1:c.8765T>G	XP_016865462.1:p.Ile2922Ser
NR_003149.2:n.15663T>G