Canonical Allele Identifier: CA9124959

Gene: KHSRP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6419244G>A , CM000681.2:g.6419244G>A	GRCh38
NC_000019.9:g.6419255G>A , CM000681.1:g.6419255G>A	GRCh37
NC_000019.8:g.6370255G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000600480.2:c.564C>T MANE Select	ENSP00000471146.2:p.Pro188=
ENST00000398148.7:c.564C>T	ENSP00000381216.2:p.Pro188=
ENST00000595112.5:n.228C>T
ENST00000595258.1:c.132C>T	ENSP00000469431.1:p.Pro44=
ENST00000595548.5:c.132C>T	ENSP00000469830.1:p.Pro44=
ENST00000599395.5:c.320C>T
ENST00000619396.4:c.564C>T	ENSP00000478033.1:p.Pro188=
NM_003685.2:c.564C>T	NP_003676.2:p.Pro188=
XM_005259668.3:c.564C>T	XP_005259725.1:p.Pro188=
XM_011528395.1:c.432C>T	XP_011526697.1:p.Pro144=
NM_001366299.1:c.564C>T MANE Select	NP_001353228.1:p.Pro188=
NM_001366300.1:c.564C>T	NP_001353229.1:p.Pro188=
XM_017027410.2:c.132C>T	XP_016882899.1:p.Pro44=
NM_003685.3:c.564C>T	NP_003676.2:p.Pro188=