Canonical Allele Identifier: CA360425750

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119394T>G (hg19) ; chr5:g.90823577T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823577T>G , CM000667.2:g.90823577T>G	GRCh38
NC_000005.9:g.90119394T>G , CM000667.1:g.90119394T>G	GRCh37
NC_000005.8:g.90155150T>G	NCBI36
NG_007083.1:g.269778T>G
NG_007083.2:g.299234T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16349T>G MANE Select	ENSP00000384582.2:p.Ile5450Ser
ENST00000425867.3:c.5303T>G	ENSP00000392618.3:p.Ile1768Ser
ENST00000638510.1:n.3616T>G
ENST00000639431.1:c.265+147368T>G	ENSP00000491057.1:n.265+147368T>G
ENST00000640061.1:n.128+1395T>G
ENST00000640407.1:c.2759T>G	ENSP00000491425.1:p.Ile920Ser
ENST00000405460.6:c.16349T>G	ENSP00000384582.2:p.Ile5450Ser
ENST00000425867.2:c.3332T>G	ENSP00000392618.2:p.Ile1111Ser
NM_032119.3:c.16349T>G	NP_115495.3:p.Ile5450Ser
NR_003149.1:n.16362T>G
XM_011543675.1:c.16346T>G	XP_011541977.1:p.Ile5449Ser
XM_011543676.1:c.16268T>G	XP_011541978.1:p.Ile5423Ser
XM_011543677.1:c.13652T>G	XP_011541979.1:p.Ile4551Ser
NM_032119.4:c.16349T>G MANE Select	NP_115495.3:p.Ile5450Ser
XM_017009963.2:c.16370T>G	XP_016865452.1:p.Ile5457Ser
XM_017009964.2:c.16367T>G	XP_016865453.1:p.Ile5456Ser
XM_017009965.1:c.16367T>G	XP_016865454.1:p.Ile5456Ser
XM_017009966.2:c.16289T>G	XP_016865455.1:p.Ile5430Ser
XM_017009967.1:c.16274T>G	XP_016865456.1:p.Ile5425Ser
XM_017009968.2:c.16190T>G	XP_016865457.1:p.Ile5397Ser
XM_017009969.2:c.16370T>G	XP_016865458.1:p.Ile5457Ser
XM_017009972.1:c.9488T>G	XP_016865461.1:p.Ile3163Ser
XM_017009973.1:c.9467T>G	XP_016865462.1:p.Ile3156Ser
NR_003149.2:n.16365T>G