Canonical Allele Identifier: CA1748724538

Gene: KEL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142958002T= , CM000669.2:g.142958002T=	GRCh38
NC_000007.13:g.142655089T= , CM000669.1:g.142655089T=	GRCh37
NC_000007.12:g.142365211T=	NCBI36
NG_007492.1:g.9415A=
NG_007492.2:g.9415A=
NG_007492.3:g.9415A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.526-29A= MANE Select	ENSP00000347409.2:n.526-29A=
ENST00000467543.6:c.*378-29A=	ENSP00000420011.2:n.*378-29A=
ENST00000355265.6:c.526-29A=	ENSP00000347409.2:n.526-29A=
ENST00000467543.5:c.469-29A=	ENSP00000420011.1:n.469-29A=
ENST00000476829.5:c.525+302A=	ENSP00000419889.1:n.525+302A=
ENST00000479768.6:n.644-29A=
ENST00000494148.1:n.125-29A=
NM_000420.2:c.526-29A=	NP_000411.1:n.526-29A=
XM_005249993.2:c.562-29A=	XP_005250050.1:n.562-29A=
NM_000420.3:c.526-29A= MANE Select	NP_000411.1:n.526-29A=