Canonical Allele Identifier: CA2136415031

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50910035A= , CM000676.2:g.50910035A=	GRCh38
NC_000014.8:g.51376753A= , CM000676.1:g.51376753A=	GRCh37
NC_000014.7:g.50446503A=	NCBI36
NG_012796.1:g.39496T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.2037T= MANE Select	ENSP00000216392.7:p.Asn679=
ENST00000216392.7:c.2037T=	ENSP00000216392.7:p.Asn679=
ENST00000532107.2:n.210T=
ENST00000532462.5:c.2037T=	ENSP00000431657.1:p.Asn679=
ENST00000544180.6:c.1935T=	ENSP00000443787.1:p.Asn645=
NM_001163940.1:c.1935T=	NP_001157412.1:p.Asn645=
NM_002863.4:c.2037T=	NP_002854.3:p.Asn679=
NM_002863.5:c.2037T= MANE Select	NP_002854.3:p.Asn679=
NM_001163940.2:c.1935T=	NP_001157412.1:p.Asn645=