Canonical Allele Identifier: CA1828293111

Gene: KCNV2 PUM3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2729612A= , CM000671.2:g.2729612A=	GRCh38
NC_000009.11:g.2729612A= , CM000671.1:g.2729612A=	GRCh37
NC_000009.10:g.2719612A=	NCBI36
NG_012181.1:g.17087A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382082.4:c.1523A= (KCNV2) MANE Select	ENSP00000371514.3:p.Tyr508=
ENST00000382082.3:c.1523A= (KCNV2)	ENSP00000371514.3:p.Tyr508=
ENST00000490444.2:c.277-9080T= (PUM3)	ENSP00000474467.1:n.277-9080T=
NM_133497.3:c.1523A= (KCNV2)	NP_598004.1:p.Tyr508=
NM_133497.4:c.1523A= (KCNV2) MANE Select	NP_598004.1:p.Tyr508=