Canonical Allele Identifier: CA388272315

Gene: TBC1D4

Linked Data

• MyVariant Identifiers: chr13:g.75884131A>G (hg19) ; chr13:g.75309995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75309995A>G , CM000675.2:g.75309995A>G	GRCh38
NC_000013.10:g.75884131A>G , CM000675.1:g.75884131A>G	GRCh37
NC_000013.9:g.74782132A>G	NCBI36
NG_042850.1:g.177174T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377636.8:c.2540T>C MANE Select	ENSP00000366863.3:p.Ile847Thr
ENST00000648194.1:c.1808T>C	ENSP00000496983.1:p.Ile603Thr
ENST00000377625.6:c.2351T>C	ENSP00000366852.2:p.Ile784Thr
ENST00000377636.7:c.2540T>C	ENSP00000366863.3:p.Ile847Thr
ENST00000431480.6:c.2516T>C	ENSP00000395986.2:p.Ile839Thr
ENST00000493487.1:n.399T>C
NM_001286658.1:c.2516T>C	NP_001273587.1:p.Ile839Thr
NM_001286658.2:c.2516T>C	NP_001273587.1:p.Ile839Thr
NM_001286659.1:c.2351T>C	NP_001273588.1:p.Ile784Thr
NM_001286659.2:c.2351T>C	NP_001273588.1:p.Ile784Thr
NM_014832.3:c.2540T>C	NP_055647.2:p.Ile847Thr
NM_014832.4:c.2540T>C	NP_055647.2:p.Ile847Thr
XM_005266603.1:c.2465T>C	XP_005266660.1:p.Ile822Thr
XM_005266605.1:c.1997T>C	XP_005266662.1:p.Ile666Thr
XM_006719903.2:c.2066T>C	XP_006719966.1:p.Ile689Thr
XM_011535331.1:c.2429T>C	XP_011533633.1:p.Ile810Thr
XM_005266603.2:c.2465T>C	XP_005266660.1:p.Ile822Thr
XM_005266605.3:c.1997T>C	XP_005266662.1:p.Ile666Thr
XM_006719903.3:c.2066T>C	XP_006719966.1:p.Ile689Thr
XM_011535331.2:c.2429T>C	XP_011533633.1:p.Ile810Thr
XM_017020882.2:c.1808T>C	XP_016876371.1:p.Ile603Thr
XM_017020883.2:c.1697T>C	XP_016876372.1:p.Ile566Thr
XM_017020884.2:c.107T>C	XP_016876373.1:p.Ile36Thr
NM_014832.5:c.2540T>C MANE Select	NP_055647.2:p.Ile847Thr