Canonical Allele Identifier: CA1562918160

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823296_90823325delinsCTATACTTTGGATGAAGAGGTACCATTTGG , CM000667.2:g.90823296_90823325delinsCTATACTTTGGATGAAGAGGTACCATTTGG	GRCh38
NC_000005.9:g.90119113_90119142delinsCTATACTTTGGATGAAGAGGTACCATTTGG , CM000667.1:g.90119113_90119142delinsCTATACTTTGGATGAAGAGGTACCATTTGG	GRCh37
NC_000005.8:g.90154869_90154898delinsCTATACTTTGGATGAAGAGGTACCATTTGG	NCBI36
NG_007083.1:g.269497_269526delinsCTATACTTTGGATGAAGAGGTACCATTTGG
NG_007083.2:g.298953_298982delinsCTATACTTTGGATGAAGAGGTACCATTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG MANE Select	ENSP00000384582.2:n.16197-129_16197-100delinsCTATACTTTGGATGAA...
ENST00000425867.3:c.5151-129_5151-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	ENSP00000392618.3:n.5151-129_5151-100delinsCTATACTTTGGATGAAGA...
ENST00000638510.1:n.3464-129_3464-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG
ENST00000639431.1:c.265+147087_265+147116delinsCTATACTTTGGATGAAGAGGTACCATTTGG	ENSP00000491057.1:n.265+147087_265+147116delinsCTATACTTTGGATG...
ENST00000640061.1:n.128+1114_128+1143delinsCTATACTTTGGATGAAGAGGTACCATTTGG
ENST00000640407.1:c.2607-129_2607-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	ENSP00000491425.1:n.2607-129_2607-100delinsCTATACTTTGGATGAAGA...
ENST00000405460.6:c.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	ENSP00000384582.2:n.16197-129_16197-100delinsCTATACTTTGGATGAA...
ENST00000425867.2:c.3180-129_3180-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	ENSP00000392618.2:n.3180-129_3180-100delinsCTATACTTTGGATGAAGA...
NM_032119.3:c.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	NP_115495.3:n.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTA...
NR_003149.1:n.16210-129_16210-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG
XM_011543675.1:c.16194-129_16194-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_011541977.1:n.16194-129_16194-100delinsCTATACTTTGGATGAAGAG...
XM_011543676.1:c.16116-129_16116-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_011541978.1:n.16116-129_16116-100delinsCTATACTTTGGATGAAGAG...
XM_011543677.1:c.13500-129_13500-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_011541979.1:n.13500-129_13500-100delinsCTATACTTTGGATGAAGAG...
NM_032119.4:c.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG MANE Select	NP_115495.3:n.16197-129_16197-100delinsCTATACTTTGGATGAAGAGGTA...
XM_017009963.2:c.16218-129_16218-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865452.1:n.16218-129_16218-100delinsCTATACTTTGGATGAAGAG...
XM_017009964.2:c.16215-129_16215-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865453.1:n.16215-129_16215-100delinsCTATACTTTGGATGAAGAG...
XM_017009965.1:c.16215-129_16215-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865454.1:n.16215-129_16215-100delinsCTATACTTTGGATGAAGAG...
XM_017009966.2:c.16137-129_16137-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865455.1:n.16137-129_16137-100delinsCTATACTTTGGATGAAGAG...
XM_017009967.1:c.16122-129_16122-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865456.1:n.16122-129_16122-100delinsCTATACTTTGGATGAAGAG...
XM_017009968.2:c.16038-129_16038-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865457.1:n.16038-129_16038-100delinsCTATACTTTGGATGAAGAG...
XM_017009969.2:c.16218-129_16218-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865458.1:n.16218-129_16218-100delinsCTATACTTTGGATGAAGAG...
XM_017009972.1:c.9336-129_9336-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865461.1:n.9336-129_9336-100delinsCTATACTTTGGATGAAGAGGT...
XM_017009973.1:c.9315-129_9315-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG	XP_016865462.1:n.9315-129_9315-100delinsCTATACTTTGGATGAAGAGGT...
NR_003149.2:n.16213-129_16213-100delinsCTATACTTTGGATGAAGAGGTACCATTTGG