Canonical Allele Identifier: CA2102696513

Gene: TBC1D4

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.75324288C= , CM000675.2:g.75324288C=	GRCh38
NC_000013.10:g.75898424C= , CM000675.1:g.75898424C=	GRCh37
NC_000013.9:g.74796425C=	NCBI36
NG_042850.1:g.162881G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377636.8:c.2147G= MANE Select	ENSP00000366863.3:p.Ser716=
ENST00000648194.1:c.1490+1909G=	ENSP00000496983.1:n.1490+1909G=
ENST00000377625.6:c.2033+1909G=	ENSP00000366852.2:n.2033+1909G=
ENST00000377636.7:c.2147G=	ENSP00000366863.3:p.Ser716=
ENST00000413735.1:c.569+1909G=	ENSP00000396932.1:n.569+1909G=
ENST00000431480.6:c.2147G=	ENSP00000395986.2:p.Ser716=
ENST00000488955.1:n.168G=
NM_001286658.1:c.2147G=	NP_001273587.1:p.Ser716=
NM_001286658.2:c.2147G=	NP_001273587.1:p.Ser716=
NM_001286659.1:c.2033+1909G=	NP_001273588.1:n.2033+1909G=
NM_001286659.2:c.2033+1909G=	NP_001273588.1:n.2033+1909G=
NM_014832.3:c.2147G=	NP_055647.2:p.Ser716=
NM_014832.4:c.2147G=	NP_055647.2:p.Ser716=
XM_005266603.1:c.2072G=	XP_005266660.1:p.Ser691=
XM_005266605.1:c.1604G=	XP_005266662.1:p.Ser535=
XM_006719903.2:c.1673G=	XP_006719966.1:p.Ser558=
XM_011535331.1:c.2036G=	XP_011533633.1:p.Ser679=
XM_005266603.2:c.2072G=	XP_005266660.1:p.Ser691=
XM_005266605.3:c.1604G=	XP_005266662.1:p.Ser535=
XM_006719903.3:c.1673G=	XP_006719966.1:p.Ser558=
XM_011535331.2:c.2036G=	XP_011533633.1:p.Ser679=
XM_017020882.2:c.1490+1909G=	XP_016876371.1:n.1490+1909G=
XM_017020883.2:c.1379+1909G=	XP_016876372.1:n.1379+1909G=
NM_014832.5:c.2147G= MANE Select	NP_055647.2:p.Ser716=