Canonical Allele Identifier: CA1748722860

Gene: KEL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.142954183C= , CM000669.2:g.142954183C=	GRCh38
NC_000007.13:g.142651270C= , CM000669.1:g.142651270C=	GRCh37
NC_000007.12:g.142361392C=	NCBI36
NG_007492.1:g.13234G=
NG_007492.2:g.13234G=
NG_007492.3:g.13234G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355265.7:c.924+1G= MANE Select	ENSP00000347409.2:n.924+1G=
ENST00000355265.6:c.924+1G=	ENSP00000347409.2:n.924+1G=
ENST00000479768.6:n.1042+1G=
NM_000420.2:c.924+1G=	NP_000411.1:n.924+1G=
XM_005249993.2:c.960+1G=	XP_005250050.1:n.960+1G=
XM_005249994.3:c.-24+1G=	XP_005250051.1:n.-24+1G=
NM_000420.3:c.924+1G= MANE Select	NP_000411.1:n.924+1G=