Canonical Allele Identifier: CA1738824733

Gene: KCND2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120665165A= , CM000669.2:g.120665165A=	GRCh38
NC_000007.13:g.120305219A= , CM000669.1:g.120305219A=	GRCh37
NC_000007.12:g.120092455A=	NCBI36
NG_034230.1:g.396498A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331113.9:c.1116-67738A= MANE Select	ENSP00000333496.4:n.1116-67738A=
ENST00000331113.8:c.1116-67738A=	ENSP00000333496.4:n.1116-67738A=
NM_012281.2:c.1116-67738A=	NP_036413.1:n.1116-67738A=
NM_012281.3:c.1116-67738A= MANE Select	NP_036413.1:n.1116-67738A=