Canonical Allele Identifier: CA2102689361

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75310080C= , CM000675.2:g.75310080C=	GRCh38
NC_000013.10:g.75884216C= , CM000675.1:g.75884216C=	GRCh37
NC_000013.9:g.74782217C=	NCBI36
NG_042850.1:g.177089G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014832.5:c.2455G= MANE Select	NP_055647.2:p.Val819=
ENST00000377636.8:c.2455G= MANE Select	ENSP00000366863.3:p.Val819=
NM_001286658.1:c.2431G=	NP_001273587.1:p.Val811=
NM_001286658.2:c.2431G=	NP_001273587.1:p.Val811=
NM_001286659.1:c.2266G=	NP_001273588.1:p.Val756=
NM_001286659.2:c.2266G=	NP_001273588.1:p.Val756=
NM_014832.3:c.2455G=	NP_055647.2:p.Val819=
NM_014832.4:c.2455G=	NP_055647.2:p.Val819=
ENST00000377625.6:c.2266G=	ENSP00000366852.2:p.Val756=
ENST00000377636.7:c.2455G=	ENSP00000366863.3:p.Val819=
ENST00000413735.1:c.802G=	ENSP00000396932.1:p.Val268=
ENST00000431480.6:c.2431G=	ENSP00000395986.2:p.Val811=
ENST00000493487.1:n.314G=
ENST00000648194.1:c.1723G=	ENSP00000496983.1:p.Val575=
XM_005266603.1:c.2380G=	XP_005266660.1:p.Val794=
XM_005266603.2:c.2380G=	XP_005266660.1:p.Val794=
XM_005266605.1:c.1912G=	XP_005266662.1:p.Val638=
XM_005266605.3:c.1912G=	XP_005266662.1:p.Val638=
XM_006719903.2:c.1981G=	XP_006719966.1:p.Val661=
XM_006719903.3:c.1981G=	XP_006719966.1:p.Val661=
XM_011535331.1:c.2344G=	XP_011533633.1:p.Val782=
XM_011535331.2:c.2344G=	XP_011533633.1:p.Val782=
XM_017020882.2:c.1723G=	XP_016876371.1:p.Val575=
XM_017020883.2:c.1612G=	XP_016876372.1:p.Val538=
XM_017020884.2:c.22G=	XP_016876373.1:p.Val8=