Canonical Allele Identifier: CA508200862

Gene: KLK3

Linked Data

• dbSNP Id: rs1183081708
• gnomAD v2: 19-51363377-C-T
• gnomAD v4: 19-50860121-C-T
• MyVariant Identifiers: chr19:g.51363377C>T (hg19) ; chr19:g.50860121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50860121C>T , CM000681.2:g.50860121C>T	GRCh38
NC_000019.9:g.51363377C>T , CM000681.1:g.51363377C>T	GRCh37
NC_000019.8:g.56055189C>T	NCBI36
NG_011653.1:g.10207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326003.7:c.780C>T MANE Select	ENSP00000314151.1:p.Asn260=
ENST00000326003.6:c.780C>T	ENSP00000314151.1:p.Asn260=
ENST00000360617.7:c.1222C>T	ENSP00000353829.2:n.1222C>T
ENST00000422986.6:c.*436C>T	ENSP00000393628.2:n.*436C>T
ENST00000595392.5:c.*281C>T	ENSP00000468912.1:n.*281C>T
ENST00000595952.5:c.651C>T	ENSP00000471155.1:p.Asn217=
ENST00000596333.1:n.958C>T
ENST00000598145.1:c.782C>T
ENST00000601349.5:n.2059C>T
ENST00000601812.1:n.1212C>T
ENST00000617027.4:c.657C>T	ENSP00000483513.1:p.Asn219=
NM_001030047.1:c.*505C>T	NP_001025218.1:n.*505C>T
NM_001030048.1:c.651C>T	NP_001025219.1:p.Asn217=
NM_001648.2:c.780C>T MANE Select	NP_001639.1:p.Asn260=
XM_011526923.1:c.798C>T	XP_011525225.1:p.Asn266=
XR_935817.1:n.1324+867C>T