Canonical Allele Identifier: CA1738824765

Gene: KCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120665201G= , CM000669.2:g.120665201G=	GRCh38
NC_000007.13:g.120305255G= , CM000669.1:g.120305255G=	GRCh37
NC_000007.12:g.120092491G=	NCBI36
NG_034230.1:g.396534G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331113.9:c.1116-67702G= MANE Select	ENSP00000333496.4:n.1116-67702G=
ENST00000331113.8:c.1116-67702G=	ENSP00000333496.4:n.1116-67702G=
NM_012281.2:c.1116-67702G=	NP_036413.1:n.1116-67702G=
NM_012281.3:c.1116-67702G= MANE Select	NP_036413.1:n.1116-67702G=