Canonical Allele Identifier: CA996827663

Gene: KLK2

Linked Data

• gnomAD v3: 19-50879814-A-ATGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGGAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAG
• gnomAD v4: 19-50879814-A-ATGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGGAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50879856_50879857insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG , CM000681.2:g.50879856_50879857insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	GRCh38
NC_000019.9:g.51383112_51383113insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG , CM000681.1:g.51383112_51383113insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	GRCh37
NC_000019.8:g.56074924_56074925insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NCBI36
NG_031984.1:g.11424_11425insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000325321.8:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG MANE Select	ENSP00000313581.2:n.*1297_*1298insAGATGAC...
ENST00000325321.7:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	ENSP00000313581.2:n.*1297_*1298insAGATGAC...
ENST00000358049.8:c.*1448_*1449insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	ENSP00000350748.3:n.*1448_*1449insAGATGAC...
ENST00000391810.6:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	ENSP00000375686.2:n.*1297_*1298insAGATGAC...
ENST00000597439.1:c.*1612_*1613insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	ENSP00000471214.1:n.*1612_*1613insAGATGAC...
NM_001002231.2:c.*1448_*1449insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NP_001002231.1:n.*1448_*1449insAGATGACATT...
NM_001256080.1:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NP_001243009.1:n.*1297_*1298insAGATGACATT...
NM_005551.4:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NP_005542.1:n.*1297_*1298insAGATGACATTTGA...
NR_045762.1:n.2148_2149insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG
NR_045763.1:n.2210_2211insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG
NM_005551.5:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG MANE Select	NP_005542.1:n.*1297_*1298insAGATGACATTTGA...
NM_001002231.3:c.*1448_*1449insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NP_001002231.1:n.*1448_*1449insAGATGACATT...
NR_045762.2:n.2142_2143insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG
NR_045763.2:n.2204_2205insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG
NM_001256080.2:c.*1297_*1298insAGATGACATTTGATTCCTTGGCATGTTCTGCCCAAGTGCCAAGGAATCAAATGTCATCTCCCAGGAGTTATTCAAGGG	NP_001243009.1:n.*1297_*1298insAGATGACATT...