Canonical Allele Identifier: CA2816822577
Gene: PCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57562821_57562822insTGGACCTCATCGCCGAGGGC , CM000682.2:g.57562821_57562822insTGGACCTCATCGCCGAGGGC GRCh38
NC_000020.10:g.56137877_56137878insTGGACCTCATCGCCGAGGGC , CM000682.1:g.56137877_56137878insTGGACCTCATCGCCGAGGGC GRCh37
NC_000020.9:g.55571283_55571284insTGGACCTCATCGCCGAGGGC NCBI36
NG_008205.1:g.6741_6742insTGGACCTCATCGCCGAGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.532_533insTGGACCTCATCGCCGAGGGC MANE Select ENSP00000319814.4:p.Thr178MetfsTer?
ENST00000319441.5:c.532_533insTGGACCTCATCGCCGAGGGC ENSP00000319814.4:p.Thr178MetfsTer?
ENST00000467047.1:n.1742_1743insTGGACCTCATCGCCGAGGGC
ENST00000498194.1:n.474_475insTGGACCTCATCGCCGAGGGC
NM_002591.3:c.532_533insTGGACCTCATCGCCGAGGGC NP_002582.3:p.Thr178MetfsTer?
XM_011528839.1:c.136_137insTGGACCTCATCGCCGAGGGC XP_011527141.1:p.Thr46MetfsTer?
XM_024451888.1:c.136_137insTGGACCTCATCGCCGAGGGC XP_024307656.1:p.Thr46MetfsTer?
NM_002591.4:c.532_533insTGGACCTCATCGCCGAGGGC MANE Select NP_002582.3:p.Thr178MetfsTer?