Canonical Allele Identifier: CA1323503833

Gene: KLF7

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.207166591G= , CM000664.2:g.207166591G=	GRCh38
NC_000002.11:g.208031315G= , CM000664.1:g.208031315G=	GRCh37
NC_000002.10:g.207739560G=	NCBI36
NG_052989.1:g.5656C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703736.1:c.3+549C=	ENSP00000515456.1:n.3+549C=
ENST00000421199.5:c.3+549C=	ENSP00000387510.1:n.3+549C=
ENST00000423015.5:c.-139+166C=	ENSP00000398572.1:n.-139+166C=
ENST00000457962.5:c.-139+403C=	ENSP00000392015.1:n.-139+403C=
NM_001270942.1:c.-139+166C=	NP_001257871.1:n.-139+166C=
NM_001270943.1:c.3+549C=	NP_001257872.1:n.3+549C=
XM_006712815.2:c.-139+166C=	XP_006712878.1:n.-139+166C=
XM_011512072.1:c.-139+403C=	XP_011510374.1:n.-139+403C=
XM_011512074.1:c.3+549C=	XP_011510376.1:n.3+549C=
XM_006712815.3:c.-139+166C=	XP_006712878.1:n.-139+166C=
XM_011512072.2:c.-139+403C=	XP_011510374.1:n.-139+403C=
XM_011512074.2:c.3+549C=	XP_011510376.1:n.3+549C=
XM_024453196.1:c.3+549C=	XP_024308964.1:n.3+549C=
NM_001270943.2:c.3+549C=	NP_001257872.1:n.3+549C=