Canonical Allele Identifier: CA309696646

Gene: KLK6

Linked Data

• dbSNP Id: rs11666929
• gnomAD v2: 19-51471648-T-C
• gnomAD v3: 19-50968392-T-C
• gnomAD v4: 19-50968392-T-C
• MyVariant Identifiers: chr19:g.51471648T>C (hg19) ; chr19:g.50968392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50968392T>C , CM000681.2:g.50968392T>C	GRCh38
NC_000019.9:g.51471648T>C , CM000681.1:g.51471648T>C	GRCh37
NC_000019.8:g.56163460T>C	NCBI36
NG_011825.1:g.6283A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310157.7:c.-9+149A>G MANE Select	ENSP00000309148.1:n.-9+149A>G
ENST00000310157.6:c.-9+149A>G	ENSP00000309148.1:n.-9+149A>G
ENST00000376851.7:c.-9+149A>G	ENSP00000366047.2:n.-9+149A>G
ENST00000376853.8:c.-9+149A>G	ENSP00000366049.4:n.-9+149A>G
ENST00000391808.5:c.-282+149A>G	ENSP00000375684.1:n.-282+149A>G
ENST00000597379.5:c.-9+149A>G	ENSP00000469630.1:n.-9+149A>G
ENST00000599690.1:c.-31+149A>G	ENSP00000469702.1:n.-31+149A>G
ENST00000599881.5:c.-9+149A>G	ENSP00000471948.1:n.-9+149A>G
NM_001012964.1:c.-9+149A>G	NP_001012982.1:n.-9+149A>G
NM_001012965.1:c.-282+149A>G	NP_001012983.1:n.-282+149A>G
NM_002774.3:c.-9+149A>G	NP_002765.1:n.-9+149A>G
XR_936036.1:n.439+39T>C
XR_936037.1:n.447+39T>C
XR_936038.1:n.439+39T>C
XR_936039.1:n.439+39T>C
XR_936040.1:n.439+39T>C
NM_001012964.2:c.-9+149A>G	NP_001012982.1:n.-9+149A>G
NM_001012965.2:c.-282+149A>G	NP_001012983.1:n.-282+149A>G
NM_001319948.1:c.-173+149A>G	NP_001306877.1:n.-173+149A>G
NM_001319949.1:c.-173+149A>G	NP_001306878.1:n.-173+149A>G
XM_024451611.1:c.-282+149A>G	XP_024307379.1:n.-282+149A>G
XR_001753976.1:n.296+39T>C
XR_001753977.1:n.304+39T>C
XR_001753978.1:n.296+39T>C
XR_001753979.1:n.296+39T>C
NM_002774.4:c.-9+149A>G MANE Select	NP_002765.1:n.-9+149A>G
NM_001319948.2:c.-173+149A>G	NP_001306877.1:n.-173+149A>G
NM_001012964.3:c.-9+149A>G	NP_001012982.1:n.-9+149A>G
NM_001012965.3:c.-282+149A>G	NP_001012983.1:n.-282+149A>G
NM_001319949.2:c.-173+149A>G	NP_001306878.1:n.-173+149A>G