Canonical Allele Identifier: CA2102689193

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75309930A= , CM000675.2:g.75309930A=	GRCh38
NC_000013.10:g.75884066A= , CM000675.1:g.75884066A=	GRCh37
NC_000013.9:g.74782067A=	NCBI36
NG_042850.1:g.177239T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377636.8:c.2593+12T= MANE Select	ENSP00000366863.3:n.2593+12T=
ENST00000648194.1:c.1861+12T=	ENSP00000496983.1:n.1861+12T=
ENST00000377625.6:c.2404+12T=	ENSP00000366852.2:n.2404+12T=
ENST00000377636.7:c.2593+12T=	ENSP00000366863.3:n.2593+12T=
ENST00000431480.6:c.2569+12T=	ENSP00000395986.2:n.2569+12T=
ENST00000493487.1:n.452+12T=
NM_001286658.1:c.2569+12T=	NP_001273587.1:n.2569+12T=
NM_001286658.2:c.2569+12T=	NP_001273587.1:n.2569+12T=
NM_001286659.1:c.2404+12T=	NP_001273588.1:n.2404+12T=
NM_001286659.2:c.2404+12T=	NP_001273588.1:n.2404+12T=
NM_014832.3:c.2593+12T=	NP_055647.2:n.2593+12T=
NM_014832.4:c.2593+12T=	NP_055647.2:n.2593+12T=
XM_005266603.1:c.2518+12T=	XP_005266660.1:n.2518+12T=
XM_005266605.1:c.2050+12T=	XP_005266662.1:n.2050+12T=
XM_006719903.2:c.2119+12T=	XP_006719966.1:n.2119+12T=
XM_011535331.1:c.2482+12T=	XP_011533633.1:n.2482+12T=
XM_005266603.2:c.2518+12T=	XP_005266660.1:n.2518+12T=
XM_005266605.3:c.2050+12T=	XP_005266662.1:n.2050+12T=
XM_006719903.3:c.2119+12T=	XP_006719966.1:n.2119+12T=
XM_011535331.2:c.2482+12T=	XP_011533633.1:n.2482+12T=
XM_017020882.2:c.1861+12T=	XP_016876371.1:n.1861+12T=
XM_017020883.2:c.1750+12T=	XP_016876372.1:n.1750+12T=
XM_017020884.2:c.160+12T=	XP_016876373.1:n.160+12T=
NM_014832.5:c.2593+12T= MANE Select	NP_055647.2:n.2593+12T=