Canonical Allele Identifier: CA388276869

Gene: TBC1D4

Linked Data

• MyVariant Identifiers: chr13:g.75898421A>T (hg19) ; chr13:g.75324285A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75324285A>T , CM000675.2:g.75324285A>T	GRCh38
NC_000013.10:g.75898421A>T , CM000675.1:g.75898421A>T	GRCh37
NC_000013.9:g.74796422A>T	NCBI36
NG_042850.1:g.162884T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377636.8:c.2150T>A MANE Select	ENSP00000366863.3:p.Phe717Tyr
ENST00000648194.1:c.1490+1912T>A	ENSP00000496983.1:n.1490+1912T>A
ENST00000377625.6:c.2033+1912T>A	ENSP00000366852.2:n.2033+1912T>A
ENST00000377636.7:c.2150T>A	ENSP00000366863.3:p.Phe717Tyr
ENST00000413735.1:c.569+1912T>A	ENSP00000396932.1:n.569+1912T>A
ENST00000431480.6:c.2150T>A	ENSP00000395986.2:p.Phe717Tyr
ENST00000488955.1:n.171T>A
NM_001286658.1:c.2150T>A	NP_001273587.1:p.Phe717Tyr
NM_001286658.2:c.2150T>A	NP_001273587.1:p.Phe717Tyr
NM_001286659.1:c.2033+1912T>A	NP_001273588.1:n.2033+1912T>A
NM_001286659.2:c.2033+1912T>A	NP_001273588.1:n.2033+1912T>A
NM_014832.3:c.2150T>A	NP_055647.2:p.Phe717Tyr
NM_014832.4:c.2150T>A	NP_055647.2:p.Phe717Tyr
XM_005266603.1:c.2075T>A	XP_005266660.1:p.Phe692Tyr
XM_005266605.1:c.1607T>A	XP_005266662.1:p.Phe536Tyr
XM_006719903.2:c.1676T>A	XP_006719966.1:p.Phe559Tyr
XM_011535331.1:c.2039T>A	XP_011533633.1:p.Phe680Tyr
XM_005266603.2:c.2075T>A	XP_005266660.1:p.Phe692Tyr
XM_005266605.3:c.1607T>A	XP_005266662.1:p.Phe536Tyr
XM_006719903.3:c.1676T>A	XP_006719966.1:p.Phe559Tyr
XM_011535331.2:c.2039T>A	XP_011533633.1:p.Phe680Tyr
XM_017020882.2:c.1490+1912T>A	XP_016876371.1:n.1490+1912T>A
XM_017020883.2:c.1379+1912T>A	XP_016876372.1:n.1379+1912T>A
NM_014832.5:c.2150T>A MANE Select	NP_055647.2:p.Phe717Tyr