Canonical Allele Identifier: CA407025224

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363366A>T (hg19) ; chr19:g.50860110A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860110A>T , CM000681.2:g.50860110A>T	GRCh38
NC_000019.9:g.51363366A>T , CM000681.1:g.51363366A>T	GRCh37
NC_000019.8:g.56055178A>T	NCBI36
NG_011653.1:g.10196A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.769A>T MANE Select	ENSP00000314151.1:p.Ile257Phe
ENST00000326003.6:c.769A>T	ENSP00000314151.1:p.Ile257Phe
ENST00000360617.7:c.1211A>T	ENSP00000353829.2:n.1211A>T
ENST00000422986.6:c.*425A>T	ENSP00000393628.2:n.*425A>T
ENST00000595392.5:c.*270A>T	ENSP00000468912.1:n.*270A>T
ENST00000595952.5:c.640A>T	ENSP00000471155.1:p.Ile214Phe
ENST00000596333.1:n.947A>T
ENST00000598145.1:c.771A>T
ENST00000601349.5:n.2048A>T
ENST00000601812.1:n.1201A>T
ENST00000617027.4:c.646A>T	ENSP00000483513.1:p.Ile216Phe
NM_001030047.1:c.*494A>T	NP_001025218.1:n.*494A>T
NM_001030048.1:c.640A>T	NP_001025219.1:p.Ile214Phe
NM_001648.2:c.769A>T MANE Select	NP_001639.1:p.Ile257Phe
XM_011526923.1:c.787A>T	XP_011525225.1:p.Ile263Phe
XR_935817.1:n.1324+856A>T