Canonical Allele Identifier: CA2466520951

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906864T= , CM000685.2:g.153906864T=	GRCh38
NC_000023.10:g.153172318T= , CM000685.1:g.153172318T=	GRCh37
NC_000023.9:g.152825512T=	NCBI36
NG_008687.1:g.6891T=
NG_009645.3:g.7360A=
NG_013220.1:g.24397A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*136T= (AVPR2) MANE Select	ENSP00000496396.1:n.*136T=
ENST00000434679.6:c.*618T= (AVPR2)	ENSP00000393397.1:n.*618T=
ENST00000642393.1:c.97+2206A=
ENST00000646191.1:c.97+2206A=
ENST00000646375.1:c.*136T= (AVPR2)	ENSP00000496396.1:n.*136T=
ENST00000337474.5:c.*136T= (AVPR2)	ENSP00000338072.5:n.*136T=
ENST00000358927.6:c.*136T= (AVPR2)	ENSP00000351805.2:n.*136T=
ENST00000434679.5:c.*618T= (AVPR2)	ENSP00000393397.1:n.*618T=
ENST00000464967.5:n.154+2206A= (L1CAM)
NM_000054.4:c.*136T= (AVPR2)	NP_000045.1:n.*136T=
NM_001146151.1:c.*428T= (AVPR2)	NP_001139623.1:n.*428T=
NR_027419.1:n.1299T= (AVPR2)
XM_006724828.2:c.*136T= (AVPR2)	XP_006724891.1:n.*136T=
NM_000054.5:c.*136T= (AVPR2)	NP_000045.1:n.*136T=
NM_001146151.2:c.*428T= (AVPR2)	NP_001139623.1:n.*428T=
XM_006724828.3:c.*136T= (AVPR2)	XP_006724891.1:n.*136T=
NM_000054.6:c.*136T= (AVPR2)	NP_000045.1:n.*136T=
NM_001146151.3:c.*428T= (AVPR2)	NP_001139623.1:n.*428T=
NR_027419.2:n.1205T= (AVPR2)
NM_000054.7:c.*136T= (AVPR2) MANE Select	NP_000045.1:n.*136T=