Canonical Allele Identifier: CA1144152

Gene: PKLR

Linked Data

• dbSNP Id: rs754970776
• ExAC: 1:155264221 A / G
• gnomAD v2: 1-155264221-A-G
• gnomAD v3: 1-155294430-A-G
• gnomAD v4: 1-155294430-A-G
• MyVariant Identifiers: chr1:g.155264221A>G (hg19) ; chr1:g.155294430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294430A>G , CM000663.2:g.155294430A>G	GRCh38
NC_000001.10:g.155264221A>G , CM000663.1:g.155264221A>G	GRCh37
NC_000001.9:g.153530845A>G	NCBI36
NG_011677.1:g.12005T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.966-45T>C MANE Select	ENSP00000339933.4:n.966-45T>C
ENST00000342741.4:c.966-45T>C	ENSP00000339933.4:n.966-45T>C
ENST00000392414.7:c.873-45T>C	ENSP00000376214.3:n.873-45T>C
NM_000298.5:c.966-45T>C	NP_000289.1:n.966-45T>C
NM_181871.3:c.873-45T>C	NP_870986.1:n.873-45T>C
XM_005245266.3:c.1125-45T>C	XP_005245323.1:n.1125-45T>C
XM_006711386.2:c.774-45T>C	XP_006711449.1:n.774-45T>C
XM_011509639.1:c.1125-45T>C	XP_011507941.1:n.1125-45T>C
XM_011509640.1:c.774-45T>C	XP_011507942.1:n.774-45T>C
NM_000298.6:c.966-45T>C MANE Select	NP_000289.1:n.966-45T>C
XM_006711386.4:c.774-45T>C	XP_006711449.1:n.774-45T>C
XM_011509640.3:c.774-45T>C	XP_011507942.1:n.774-45T>C
XM_017001493.1:c.966-45T>C	XP_016856982.1:n.966-45T>C
NM_181871.4:c.873-45T>C	NP_870986.1:n.873-45T>C