Canonical Allele Identifier: CA9604606

Gene: KLK3

Linked Data

• dbSNP Id: rs548476435
• ExAC: 19:51363354 A / T
• gnomAD v2: 19-51363354-A-T
• gnomAD v4: 19-50860098-A-T
• MyVariant Identifiers: chr19:g.51363354A>T (hg19) ; chr19:g.50860098A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860098A>T , CM000681.2:g.50860098A>T	GRCh38
NC_000019.9:g.51363354A>T , CM000681.1:g.51363354A>T	GRCh37
NC_000019.8:g.56055166A>T	NCBI36
NG_011653.1:g.10184A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.757A>T MANE Select	ENSP00000314151.1:p.Ile253Phe
ENST00000326003.6:c.757A>T	ENSP00000314151.1:p.Ile253Phe
ENST00000360617.7:c.1199A>T	ENSP00000353829.2:n.1199A>T
ENST00000422986.6:c.*413A>T	ENSP00000393628.2:n.*413A>T
ENST00000595392.5:c.*258A>T	ENSP00000468912.1:n.*258A>T
ENST00000595952.5:c.628A>T	ENSP00000471155.1:p.Ile210Phe
ENST00000596333.1:n.935A>T
ENST00000598145.1:c.759A>T
ENST00000601349.5:n.2036A>T
ENST00000601812.1:n.1189A>T
ENST00000617027.4:c.634A>T	ENSP00000483513.1:p.Ile212Phe
NM_001030047.1:c.*482A>T	NP_001025218.1:n.*482A>T
NM_001030048.1:c.628A>T	NP_001025219.1:p.Ile210Phe
NM_001648.2:c.757A>T MANE Select	NP_001639.1:p.Ile253Phe
XM_011526923.1:c.775A>T	XP_011525225.1:p.Ile259Phe
XR_935817.1:n.1324+844A>T