Canonical Allele Identifier: CA2466520354

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153905325_153905343delinsAGGGCTGGGGCTGGGGCTG , CM000685.2:g.153905325_153905343delinsAGGGCTGGGGCTGGGGCTG	GRCh38
NC_000023.10:g.153170779_153170797delinsAGGGCTGGGGCTGGGGCTG , CM000685.1:g.153170779_153170797delinsAGGGCTGGGGCTGGGGCTG	GRCh37
NC_000023.9:g.152823973_152823991delinsAGGGCTGGGGCTGGGGCTG	NCBI36
NG_008687.1:g.5352_5370delinsAGGGCTGGGGCTGGGGCTG
NG_009645.3:g.8881_8899delinsCAGCCCCAGCCCCAGCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2) MANE Select	ENSP00000496396.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000434679.6:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000393397.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000642393.1:c.97+3727_97+3745delinsCAGCCCCAGCCCCAGCCCT
ENST00000646191.1:c.97+3727_97+3745delinsCAGCCCCAGCCCCAGCCCT
ENST00000646375.1:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000496396.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000337474.5:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000338072.5:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000358927.6:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000351805.2:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000370049.1:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000359066.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000430697.1:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000393513.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000434679.5:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	ENSP00000393397.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
ENST00000464967.5:n.154+3727_154+3745delinsCAGCCCCAGCCCCAGCCCT (L1CAM)
NM_000054.4:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_000045.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NM_001146151.1:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_001139623.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NR_027419.1:n.559+155_559+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)
XM_006724828.2:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	XP_006724891.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NM_000054.5:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_000045.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NM_001146151.2:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_001139623.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
XM_006724828.3:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	XP_006724891.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NM_000054.6:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_000045.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NM_001146151.3:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)	NP_001139623.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG
NR_027419.2:n.465+155_465+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2)
NM_000054.7:c.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG (AVPR2) MANE Select	NP_000045.1:n.25+155_25+173delinsAGGGCTGGGGCTGGGGCTG