Canonical Allele Identifier: CA1200112304

Gene: PKLR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294782_155294783delinsCA , CM000663.2:g.155294782_155294783delinsCA	GRCh38
NC_000001.10:g.155264573_155264574delinsCA , CM000663.1:g.155264573_155264574delinsCA	GRCh37
NC_000001.9:g.153531197_153531198delinsCA	NCBI36
NG_011677.1:g.11652_11653delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.695-31_695-30delinsTG MANE Select	ENSP00000339933.4:n.695-31_695-30delinsTG
ENST00000342741.4:c.695-31_695-30delinsTG	ENSP00000339933.4:n.695-31_695-30delinsTG
ENST00000392414.7:c.602-31_602-30delinsTG	ENSP00000376214.3:n.602-31_602-30delinsTG
NM_000298.5:c.695-31_695-30delinsTG	NP_000289.1:n.695-31_695-30delinsTG
NM_181871.3:c.602-31_602-30delinsTG	NP_870986.1:n.602-31_602-30delinsTG
XM_005245266.3:c.854-31_854-30delinsTG	XP_005245323.1:n.854-31_854-30delinsTG
XM_006711386.2:c.503-31_503-30delinsTG	XP_006711449.1:n.503-31_503-30delinsTG
XM_011509639.1:c.854-31_854-30delinsTG	XP_011507941.1:n.854-31_854-30delinsTG
XM_011509640.1:c.503-31_503-30delinsTG	XP_011507942.1:n.503-31_503-30delinsTG
NM_000298.6:c.695-31_695-30delinsTG MANE Select	NP_000289.1:n.695-31_695-30delinsTG
XM_006711386.4:c.503-31_503-30delinsTG	XP_006711449.1:n.503-31_503-30delinsTG
XM_011509640.3:c.503-31_503-30delinsTG	XP_011507942.1:n.503-31_503-30delinsTG
XM_017001493.1:c.695-31_695-30delinsTG	XP_016856982.1:n.695-31_695-30delinsTG
NM_181871.4:c.602-31_602-30delinsTG	NP_870986.1:n.602-31_602-30delinsTG