Canonical Allele Identifier: CA421020448

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264527C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294736C>A , CM000663.2:g.155294736C>A	GRCh38
NC_000001.10:g.155264527C>A , CM000663.1:g.155264527C>A	GRCh37
NC_000001.9:g.153531151C>A	NCBI36
NG_011677.1:g.11699G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342741.6:c.711G>T MANE Select	ENSP00000339933.4:p.Val237=
ENST00000342741.4:c.711G>T	ENSP00000339933.4:p.Val237=
ENST00000392414.7:c.618G>T	ENSP00000376214.3:p.Val206=
NM_000298.5:c.711G>T	NP_000289.1:p.Val237=
NM_181871.3:c.618G>T	NP_870986.1:p.Val206=
XM_005245266.3:c.870G>T	XP_005245323.1:p.Val290=
XM_006711386.2:c.519G>T	XP_006711449.1:p.Val173=
XM_011509639.1:c.870G>T	XP_011507941.1:p.Val290=
XM_011509640.1:c.519G>T	XP_011507942.1:p.Val173=
NM_000298.6:c.711G>T MANE Select	NP_000289.1:p.Val237=
XM_006711386.4:c.519G>T	XP_006711449.1:p.Val173=
XM_011509640.3:c.519G>T	XP_011507942.1:p.Val173=
XM_017001493.1:c.711G>T	XP_016856982.1:p.Val237=
NM_181871.4:c.618G>T	NP_870986.1:p.Val206=