Canonical Allele Identifier: CA2081142138

Gene: POMP

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659438T= , CM000675.2:g.28659438T=	GRCh38
NC_000013.10:g.29233575T= , CM000675.1:g.29233575T=	GRCh37
NC_000013.9:g.28131575T=	NCBI36
NG_027550.1:g.5435T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+251T=	ENSP00000513386.1:n.-246+251T=
ENST00000697662.1:c.-282+251T=	ENSP00000513387.1:n.-282+251T=
ENST00000697716.1:c.-83+251T=	ENSP00000513414.1:n.-83+251T=
ENST00000697717.1:c.3+251T=	ENSP00000513415.1:n.3+251T=
ENST00000697718.1:c.3+251T=	ENSP00000513416.1:n.3+251T=
ENST00000697719.1:c.-301T=	ENSP00000513417.1:n.-301T=
ENST00000697720.1:c.-459T=	ENSP00000513418.1:n.-459T=
ENST00000380842.5:c.3+251T= MANE Select	ENSP00000370222.4:n.3+251T=
ENST00000380842.4:c.3+251T=	ENSP00000370222.4:n.3+251T=
ENST00000460403.1:n.84+251T=
NM_015932.5:c.3+251T=	NP_057016.1:n.3+251T=
XR_941802.1:n.244T=
NM_015932.6:c.3+251T= MANE Select	NP_057016.1:n.3+251T=