Canonical Allele Identifier: CA214730

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75481684G>C , CM000675.2:g.75481684G>C	GRCh38
NC_000013.10:g.76055820G>C , CM000675.1:g.76055820G>C	GRCh37
NC_000013.9:g.74953821G>C	NCBI36
NG_042850.1:g.5485C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377636.8:c.84C>G MANE Select	ENSP00000366863.3:p.Pro28=
ENST00000377625.6:c.84C>G	ENSP00000366852.2:p.Pro28=
ENST00000377636.7:c.84C>G	ENSP00000366863.3:p.Pro28=
ENST00000431480.6:c.84C>G	ENSP00000395986.2:p.Pro28=
NM_001286658.1:c.84C>G	NP_001273587.1:p.Pro28=
NM_001286658.2:c.84C>G	NP_001273587.1:p.Pro28=
NM_001286659.1:c.84C>G	NP_001273588.1:p.Pro28=
NM_001286659.2:c.84C>G	NP_001273588.1:p.Pro28=
NM_014832.3:c.84C>G	NP_055647.2:p.Pro28=
NM_014832.4:c.84C>G	NP_055647.2:p.Pro28=
XM_005266603.1:c.84C>G	XP_005266660.1:p.Pro28=
XM_011535331.1:c.84C>G	XP_011533633.1:p.Pro28=
XM_005266603.2:c.84C>G	XP_005266660.1:p.Pro28=
XM_011535331.2:c.84C>G	XP_011533633.1:p.Pro28=
NM_014832.5:c.84C>G MANE Select	NP_055647.2:p.Pro28=