Canonical Allele Identifier: CA2250570600

Gene: PEMT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17506250G= , CM000679.2:g.17506250G=	GRCh38
NC_000017.10:g.17409564G= , CM000679.1:g.17409564G=	GRCh37
NC_000017.9:g.17350289G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000255389.10:c.630C= MANE Select	ENSP00000255389.5:p.Tyr210=
ENST00000255389.9:c.630C=	ENSP00000255389.5:p.Tyr210=
ENST00000395781.6:c.661C=	ENSP00000379127.2:p.His221=
ENST00000395782.5:c.519C=	ENSP00000379128.1:p.Tyr173=
ENST00000395783.5:c.519C=	ENSP00000379129.1:p.Tyr173=
ENST00000435340.6:c.598C=	ENSP00000391288.2:p.His200=
ENST00000477595.5:n.124C=
ENST00000484838.6:n.494C=
ENST00000490392.5:n.364C=
ENST00000580147.5:c.*128C=	ENSP00000463112.1:n.*128C=
ENST00000582268.5:n.74C=
NM_001267551.1:c.564C=	NP_001254480.1:p.Tyr188=
NM_001267552.1:c.661C=	NP_001254481.1:p.His221=
NM_007169.2:c.519C=	NP_009100.2:p.Tyr173=
NM_148172.2:c.630C=	NP_680477.1:p.Tyr210=
NM_148173.1:c.519C=	NP_680478.1:p.Tyr173=
XM_006721418.2:c.567C=	XP_006721481.2:p.Tyr189=
XM_006721418.4:c.567C=	XP_006721481.2:p.Tyr189=
XM_017024016.1:c.297C=	XP_016879505.1:p.Tyr99=
XM_024450532.1:c.519C=	XP_024306300.1:p.Tyr173=
NM_148172.3:c.630C= MANE Select	NP_680477.1:p.Tyr210=
NM_001267551.2:c.564C=	NP_001254480.1:p.Tyr188=
NM_001267552.2:c.661C=	NP_001254481.1:p.His221=
NM_007169.3:c.519C=	NP_009100.2:p.Tyr173=
NM_148173.2:c.519C=	NP_680478.1:p.Tyr173=