Canonical Allele Identifier: CA726623068

Gene: PEMT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17588763G>A , CM000679.2:g.17588763G>A	GRCh38
NC_000017.10:g.17492077G>A , CM000679.1:g.17492077G>A	GRCh37
NC_000017.9:g.17432802G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255389.10:c.96+2768C>T MANE Select	ENSP00000255389.5:n.96+2768C>T
ENST00000255389.9:c.96+2768C>T	ENSP00000255389.5:n.96+2768C>T
ENST00000395781.6:c.96+2768C>T	ENSP00000379127.2:n.96+2768C>T
ENST00000421096.5:n.120+2768C>T
ENST00000435340.6:c.30+2834C>T	ENSP00000391288.2:n.30+2834C>T
ENST00000461404.1:c.96+2768C>T	ENSP00000463713.1:n.96+2768C>T
ENST00000472446.1:n.107+2834C>T
ENST00000580147.5:c.96+2768C>T	ENSP00000463112.1:n.96+2768C>T
NM_001267551.1:c.30+2834C>T	NP_001254480.1:n.30+2834C>T
NM_001267552.1:c.96+2768C>T	NP_001254481.1:n.96+2768C>T
NM_148172.2:c.96+2768C>T	NP_680477.1:n.96+2768C>T
XM_024450532.1:c.-16+3204C>T	XP_024306300.1:n.-16+3204C>T
NM_148172.3:c.96+2768C>T MANE Select	NP_680477.1:n.96+2768C>T
NM_001267551.2:c.30+2834C>T	NP_001254480.1:n.30+2834C>T
NM_001267552.2:c.96+2768C>T	NP_001254481.1:n.96+2768C>T