Canonical Allele Identifier: CA252117846

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75289179G>C , CM000675.2:g.75289179G>C	GRCh38
NC_000013.10:g.75863315G>C , CM000675.1:g.75863315G>C	GRCh37
NC_000013.9:g.74761316G>C	NCBI36
NG_042850.1:g.197990C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014832.5:c.3487-69C>G MANE Select	NP_055647.2:n.3487-69C>G
ENST00000377636.8:c.3487-69C>G MANE Select	ENSP00000366863.3:n.3487-69C>G
NM_001286658.1:c.3463-69C>G	NP_001273587.1:n.3463-69C>G
NM_001286658.2:c.3463-69C>G	NP_001273587.1:n.3463-69C>G
NM_001286659.1:c.3298-69C>G	NP_001273588.1:n.3298-69C>G
NM_001286659.2:c.3298-69C>G	NP_001273588.1:n.3298-69C>G
NM_014832.3:c.3487-69C>G	NP_055647.2:n.3487-69C>G
NM_014832.4:c.3487-69C>G	NP_055647.2:n.3487-69C>G
ENST00000377625.6:c.3298-69C>G	ENSP00000366852.2:n.3298-69C>G
ENST00000377636.7:c.3487-69C>G	ENSP00000366863.3:n.3487-69C>G
ENST00000431480.6:c.3463-69C>G	ENSP00000395986.2:n.3463-69C>G
ENST00000648194.1:c.2755-69C>G	ENSP00000496983.1:n.2755-69C>G
XM_005266603.1:c.3412-69C>G	XP_005266660.1:n.3412-69C>G
XM_005266603.2:c.3412-69C>G	XP_005266660.1:n.3412-69C>G
XM_005266605.1:c.2944-69C>G	XP_005266662.1:n.2944-69C>G
XM_005266605.3:c.2944-69C>G	XP_005266662.1:n.2944-69C>G
XM_006719903.2:c.3013-69C>G	XP_006719966.1:n.3013-69C>G
XM_006719903.3:c.3013-69C>G	XP_006719966.1:n.3013-69C>G
XM_011535331.1:c.3376-69C>G	XP_011533633.1:n.3376-69C>G
XM_011535331.2:c.3376-69C>G	XP_011533633.1:n.3376-69C>G
XM_017020882.2:c.2755-69C>G	XP_016876371.1:n.2755-69C>G
XM_017020883.2:c.2644-69C>G	XP_016876372.1:n.2644-69C>G
XM_017020884.2:c.1054-69C>G	XP_016876373.1:n.1054-69C>G