Canonical Allele Identifier: CA2102689261

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75309993G= , CM000675.2:g.75309993G=	GRCh38
NC_000013.10:g.75884129G= , CM000675.1:g.75884129G=	GRCh37
NC_000013.9:g.74782130G=	NCBI36
NG_042850.1:g.177176C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377636.8:c.2542C= MANE Select	ENSP00000366863.3:p.His848=
ENST00000648194.1:c.1810C=	ENSP00000496983.1:p.His604=
ENST00000377625.6:c.2353C=	ENSP00000366852.2:p.His785=
ENST00000377636.7:c.2542C=	ENSP00000366863.3:p.His848=
ENST00000431480.6:c.2518C=	ENSP00000395986.2:p.His840=
ENST00000493487.1:n.401C=
NM_001286658.1:c.2518C=	NP_001273587.1:p.His840=
NM_001286658.2:c.2518C=	NP_001273587.1:p.His840=
NM_001286659.1:c.2353C=	NP_001273588.1:p.His785=
NM_001286659.2:c.2353C=	NP_001273588.1:p.His785=
NM_014832.3:c.2542C=	NP_055647.2:p.His848=
NM_014832.4:c.2542C=	NP_055647.2:p.His848=
XM_005266603.1:c.2467C=	XP_005266660.1:p.His823=
XM_005266605.1:c.1999C=	XP_005266662.1:p.His667=
XM_006719903.2:c.2068C=	XP_006719966.1:p.His690=
XM_011535331.1:c.2431C=	XP_011533633.1:p.His811=
XM_005266603.2:c.2467C=	XP_005266660.1:p.His823=
XM_005266605.3:c.1999C=	XP_005266662.1:p.His667=
XM_006719903.3:c.2068C=	XP_006719966.1:p.His690=
XM_011535331.2:c.2431C=	XP_011533633.1:p.His811=
XM_017020882.2:c.1810C=	XP_016876371.1:p.His604=
XM_017020883.2:c.1699C=	XP_016876372.1:p.His567=
XM_017020884.2:c.109C=	XP_016876373.1:p.His37=
NM_014832.5:c.2542C= MANE Select	NP_055647.2:p.His848=