Canonical Allele Identifier: CA407025079

Gene: KLK3

Linked Data

• MyVariant Identifiers: chr19:g.51363318T>C (hg19) ; chr19:g.50860062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860062T>C , CM000681.2:g.50860062T>C	GRCh38
NC_000019.9:g.51363318T>C , CM000681.1:g.51363318T>C	GRCh37
NC_000019.8:g.56055130T>C	NCBI36
NG_011653.1:g.10148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.721T>C MANE Select	ENSP00000314151.1:p.Ser241Pro
ENST00000326003.6:c.721T>C	ENSP00000314151.1:p.Ser241Pro
ENST00000360617.7:c.1163T>C	ENSP00000353829.2:n.1163T>C
ENST00000422986.6:c.*377T>C	ENSP00000393628.2:n.*377T>C
ENST00000595392.5:c.*222T>C	ENSP00000468912.1:n.*222T>C
ENST00000595952.5:c.592T>C	ENSP00000471155.1:p.Ser198Pro
ENST00000596333.1:n.899T>C
ENST00000598145.1:c.723T>C
ENST00000601349.5:n.2000T>C
ENST00000601812.1:n.1153T>C
ENST00000617027.4:c.598T>C	ENSP00000483513.1:p.Ser200Pro
NM_001030047.1:c.*446T>C	NP_001025218.1:n.*446T>C
NM_001030048.1:c.592T>C	NP_001025219.1:p.Ser198Pro
NM_001648.2:c.721T>C MANE Select	NP_001639.1:p.Ser241Pro
XM_011526923.1:c.739T>C	XP_011525225.1:p.Ser247Pro
XR_935817.1:n.1324+808T>C