Canonical Allele Identifier: CA2343362709

Gene: TMEM150B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55322296A= , CM000681.2:g.55322296A=	GRCh38
NC_000019.9:g.55833664A= , CM000681.1:g.55833664A=	GRCh37
NC_000019.8:g.60525476A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001282011.2:c.-58+352T= MANE Select	NP_001268940.1:n.-58+352T=
ENST00000326652.9:c.-58+352T= MANE Select	ENSP00000320757.4:n.-58+352T=
NM_001085488.2:c.-9+352T=	NP_001078957.1:n.-9+352T=
NM_001085488.3:c.-9+352T=	NP_001078957.1:n.-9+352T=
NM_001282011.1:c.-58+352T=	NP_001268940.1:n.-58+352T=
NR_104066.1:n.165+352T=
NR_104066.2:n.166+352T=
NR_104071.1:n.165+352T=
NR_104071.2:n.166+352T=
ENST00000326652.8:c.-58+352T=	ENSP00000320757.4:n.-58+352T=
ENST00000586609.5:c.-58+352T=	ENSP00000466957.1:n.-58+352T=
ENST00000591570.5:c.-9+352T=	ENSP00000466297.1:n.-9+352T=
ENST00000592603.5:c.-9+352T=	ENSP00000468745.1:n.-9+352T=
ENST00000592731.5:c.-8-1252T=	ENSP00000465815.1:n.-8-1252T=
ENST00000592891.1:n.241+352T=
XM_005258812.2:c.-58+352T=	XP_005258869.1:n.-58+352T=
XM_005258812.4:c.-58+352T=	XP_005258869.1:n.-58+352T=
XM_011526850.3:c.-58+352T=	XP_011525152.1:n.-58+352T=
XM_011526851.3:c.-58+352T=	XP_011525153.1:n.-58+352T=
XM_011526852.1:c.-58+352T=	XP_011525154.1:n.-58+352T=
XM_011526852.3:c.-58+352T=	XP_011525154.1:n.-58+352T=
XM_011526853.1:c.-58+352T=	XP_011525155.1:n.-58+352T=
XM_011526853.2:c.-58+352T=	XP_011525155.1:n.-58+352T=
XM_011526855.1:c.-9+352T=	XP_011525157.1:n.-9+352T=
XM_011526855.3:c.-9+352T=	XP_011525157.1:n.-9+352T=
XM_017026667.2:c.-72+352T=	XP_016882156.1:n.-72+352T=