Canonical Allele Identifier: CA8567194

Gene: KLHL10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41841889C>T , CM000679.2:g.41841889C>T	GRCh38
NC_000017.10:g.39998141C>T , CM000679.1:g.39998141C>T	GRCh37
NC_000017.9:g.37251667C>T	NCBI36
NG_051246.1:g.11205C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_152467.5:c.261C>T MANE Select	NP_689680.2:p.Pro87=
ENST00000293303.5:c.261C>T MANE Select	ENSP00000293303.4:p.Pro87=
NM_001329595.1:c.261C>T	NP_001316524.1:p.Pro87=
NM_001329596.1:c.-4C>T	NP_001316525.1:n.-4C>T
NM_001329596.2:c.-4C>T	NP_001316525.1:n.-4C>T
NM_152467.3:c.261C>T	NP_689680.2:p.Pro87=
NM_152467.4:c.261C>T	NP_689680.2:p.Pro87=
ENST00000293303.4:c.261C>T	ENSP00000293303.4:p.Pro87=
ENST00000438813.1:c.243C>T	ENSP00000416221.1:p.Pro81=
ENST00000448203.2:c.261C>T	ENSP00000391983.2:p.Pro87=
ENST00000485613.1:n.307C>T
XM_011524706.1:c.261C>T	XP_011523008.1:p.Pro87=