Canonical Allele Identifier: CA2695073693

Gene: AVPR2 L1CAM

Linked Data

• gnomAD v4: X-153906837-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906838del , CM000685.2:g.153906838del	GRCh38
NC_000023.10:g.153172292del , CM000685.1:g.153172292del	GRCh37
NC_000023.9:g.152825486del	NCBI36
NG_008687.1:g.6865del
NG_009645.3:g.7386del
NG_013220.1:g.24423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*110del (AVPR2) MANE Select	ENSP00000496396.1:n.*110del
ENST00000434679.6:c.*592del (AVPR2)	ENSP00000393397.1:n.*592del
ENST00000642393.1:c.97+2232del
ENST00000646191.1:c.97+2232del
ENST00000646375.1:c.*110del (AVPR2)	ENSP00000496396.1:n.*110del
ENST00000337474.5:c.*110del (AVPR2)	ENSP00000338072.5:n.*110del
ENST00000358927.6:c.*110del (AVPR2)	ENSP00000351805.2:n.*110del
ENST00000434679.5:c.*592del (AVPR2)	ENSP00000393397.1:n.*592del
ENST00000464967.5:n.154+2232del (L1CAM)
NM_000054.4:c.*110del (AVPR2)	NP_000045.1:n.*110del
NM_001146151.1:c.*402del (AVPR2)	NP_001139623.1:n.*402del
NR_027419.1:n.1273del (AVPR2)
XM_006724828.2:c.*110del (AVPR2)	XP_006724891.1:n.*110del
NM_000054.5:c.*110del (AVPR2)	NP_000045.1:n.*110del
NM_001146151.2:c.*402del (AVPR2)	NP_001139623.1:n.*402del
XM_006724828.3:c.*110del (AVPR2)	XP_006724891.1:n.*110del
NM_000054.6:c.*110del (AVPR2)	NP_000045.1:n.*110del
NM_001146151.3:c.*402del (AVPR2)	NP_001139623.1:n.*402del
NR_027419.2:n.1179del (AVPR2)
NM_000054.7:c.*110del (AVPR2) MANE Select	NP_000045.1:n.*110del