Canonical Allele Identifier: CA2399923342

Gene: TTC28 TTC28-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.27982484A= , CM000684.2:g.27982484A=	GRCh38
NC_000022.10:g.28378472A= , CM000684.1:g.28378472A=	GRCh37
NC_000022.9:g.26708472A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001145418.2:c.7183T= (TTC28) MANE Select	NP_001138890.1:p.Leu2395=
ENST00000397906.7:c.7183T= (TTC28) MANE Select	ENSP00000381003.2:p.Leu2395=
NM_001145418.1:c.7183T= (TTC28)	NP_001138890.1:p.Leu2395=
NM_001393403.1:c.7159T= (TTC28)	NP_001380332.1:p.Leu2387=
NM_001393404.1:c.6829T= (TTC28)	NP_001380333.1:p.Leu2277=
NM_001393405.1:c.6805T= (TTC28)	NP_001380334.1:p.Leu2269=
NR_026963.1:n.251-11989A= (TTC28-AS1)
ENST00000397906.6:c.7183T= (TTC28)	ENSP00000381003.2:p.Leu2395=
ENST00000612946.4:c.6802T= (TTC28)	ENSP00000479834.1:p.Leu2268=
XM_005261405.2:c.7159T= (TTC28)	XP_005261462.1:p.Leu2387=
XM_006724171.2:c.6829T= (TTC28)	XP_006724234.1:p.Leu2277=
XM_006724171.4:c.6829T= (TTC28)	XP_006724234.1:p.Leu2277=
XM_011530018.1:c.7105T= (TTC28)	XP_011528320.1:p.Leu2369=
XM_011530018.3:c.7105T= (TTC28)	XP_011528320.1:p.Leu2369=
XM_017028673.2:c.7093T= (TTC28)	XP_016884162.1:p.Leu2365=