Canonical Allele Identifier: CA398543065

Gene: PEMT

Linked Data

• gnomAD v4: 17-17506254-G-T
• MyVariant Identifiers: chr17:g.17409568G>T (hg19) ; chr17:g.17506254G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17506254G>T , CM000679.2:g.17506254G>T	GRCh38
NC_000017.10:g.17409568G>T , CM000679.1:g.17409568G>T	GRCh37
NC_000017.9:g.17350293G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000255389.10:c.626C>A MANE Select	ENSP00000255389.5:p.Thr209Asn
ENST00000255389.9:c.626C>A	ENSP00000255389.5:p.Thr209Asn
ENST00000395781.6:c.657C>A	ENSP00000379127.2:p.His219Gln
ENST00000395782.5:c.515C>A	ENSP00000379128.1:p.Thr172Asn
ENST00000395783.5:c.515C>A	ENSP00000379129.1:p.Thr172Asn
ENST00000435340.6:c.594C>A	ENSP00000391288.2:p.His198Gln
ENST00000477595.5:n.120C>A
ENST00000484838.6:n.490C>A
ENST00000490392.5:n.360C>A
ENST00000580147.5:c.*124C>A	ENSP00000463112.1:n.*124C>A
ENST00000582268.5:n.70C>A
NM_001267551.1:c.560C>A	NP_001254480.1:p.Thr187Asn
NM_001267552.1:c.657C>A	NP_001254481.1:p.His219Gln
NM_007169.2:c.515C>A	NP_009100.2:p.Thr172Asn
NM_148172.2:c.626C>A	NP_680477.1:p.Thr209Asn
NM_148173.1:c.515C>A	NP_680478.1:p.Thr172Asn
XM_006721418.2:c.563C>A	XP_006721481.2:p.Thr188Asn
XM_006721418.4:c.563C>A	XP_006721481.2:p.Thr188Asn
XM_017024016.1:c.293C>A	XP_016879505.1:p.Thr98Asn
XM_024450532.1:c.515C>A	XP_024306300.1:p.Thr172Asn
NM_148172.3:c.626C>A MANE Select	NP_680477.1:p.Thr209Asn
NM_001267551.2:c.560C>A	NP_001254480.1:p.Thr187Asn
NM_001267552.2:c.657C>A	NP_001254481.1:p.His219Gln
NM_007169.3:c.515C>A	NP_009100.2:p.Thr172Asn
NM_148173.2:c.515C>A	NP_680478.1:p.Thr172Asn