Canonical Allele Identifier: CA13847617

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75326756C>T , CM000675.2:g.75326756C>T	GRCh38
NC_000013.10:g.75900892C>T , CM000675.1:g.75900892C>T	GRCh37
NC_000013.9:g.74798893C>T	NCBI36
NG_042850.1:g.160413G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014832.5:c.1807-333G>A MANE Select	NP_055647.2:n.1807-333G>A
ENST00000377636.8:c.1807-333G>A MANE Select	ENSP00000366863.3:n.1807-333G>A
NM_001286658.1:c.1807-333G>A	NP_001273587.1:n.1807-333G>A
NM_001286658.2:c.1807-333G>A	NP_001273587.1:n.1807-333G>A
NM_001286659.1:c.1807-333G>A	NP_001273588.1:n.1807-333G>A
NM_001286659.2:c.1807-333G>A	NP_001273588.1:n.1807-333G>A
NM_014832.3:c.1807-333G>A	NP_055647.2:n.1807-333G>A
NM_014832.4:c.1807-333G>A	NP_055647.2:n.1807-333G>A
ENST00000377625.6:c.1807-333G>A	ENSP00000366852.2:n.1807-333G>A
ENST00000377636.7:c.1807-333G>A	ENSP00000366863.3:n.1807-333G>A
ENST00000413735.1:c.343-333G>A	ENSP00000396932.1:n.343-333G>A
ENST00000431480.6:c.1807-333G>A	ENSP00000395986.2:n.1807-333G>A
ENST00000648194.1:c.1264-333G>A	ENSP00000496983.1:n.1264-333G>A
XM_005266603.1:c.1732-333G>A	XP_005266660.1:n.1732-333G>A
XM_005266603.2:c.1732-333G>A	XP_005266660.1:n.1732-333G>A
XM_005266605.1:c.1264-333G>A	XP_005266662.1:n.1264-333G>A
XM_005266605.3:c.1264-333G>A	XP_005266662.1:n.1264-333G>A
XM_006719903.2:c.1333-333G>A	XP_006719966.1:n.1333-333G>A
XM_006719903.3:c.1333-333G>A	XP_006719966.1:n.1333-333G>A
XM_011535331.1:c.1696-333G>A	XP_011533633.1:n.1696-333G>A
XM_011535331.2:c.1696-333G>A	XP_011533633.1:n.1696-333G>A
XM_017020882.2:c.1264-333G>A	XP_016876371.1:n.1264-333G>A
XM_017020883.2:c.1153-333G>A	XP_016876372.1:n.1153-333G>A