Canonical Allele Identifier: CA2399977644

Gene: TTC28

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.28105426C= , CM000684.2:g.28105426C=	GRCh38
NC_000022.10:g.28501414C= , CM000684.1:g.28501414C=	GRCh37
NC_000022.9:g.26831414C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001145418.2:c.3160G= MANE Select	NP_001138890.1:p.Glu1054=
ENST00000397906.7:c.3160G= MANE Select	ENSP00000381003.2:p.Glu1054=
NM_001145418.1:c.3160G=	NP_001138890.1:p.Glu1054=
NM_001393403.1:c.3160G=	NP_001380332.1:p.Glu1054=
NM_001393404.1:c.2806G=	NP_001380333.1:p.Glu936=
NM_001393405.1:c.2806G=	NP_001380334.1:p.Glu936=
ENST00000397906.6:c.3160G=	ENSP00000381003.2:p.Glu1054=
ENST00000612946.4:c.2779G=	ENSP00000479834.1:p.Glu927=
XM_005261405.2:c.3160G=	XP_005261462.1:p.Glu1054=
XM_006724171.2:c.2806G=	XP_006724234.1:p.Glu936=
XM_006724171.4:c.2806G=	XP_006724234.1:p.Glu936=
XM_011530018.1:c.3082G=	XP_011528320.1:p.Glu1028=
XM_011530018.3:c.3082G=	XP_011528320.1:p.Glu1028=
XM_011530019.1:c.3160G=	XP_011528321.1:p.Glu1054=
XM_011530019.2:c.3160G=	XP_011528321.1:p.Glu1054=
XM_011530020.1:c.3160G=	XP_011528322.1:p.Glu1054=
XM_011530021.1:c.3160G=	XP_011528323.1:p.Glu1054=
XM_011530021.3:c.3160G=	XP_011528323.1:p.Glu1054=
XM_011530022.1:c.3160G=	XP_011528324.1:p.Glu1054=
XM_017028673.2:c.3070G=	XP_016884162.1:p.Glu1024=