Canonical Allele Identifier: CA1929655140

Gene: TCTN3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686504C= , CM000672.2:g.95686504C=	GRCh38
NC_000010.10:g.97446261C= , CM000672.1:g.97446261C=	GRCh37
NC_000010.9:g.97436251C=	NCBI36
NG_032953.1:g.12640G=

Transcript Alleles

HGVS	Amino-acid Change
NM_015631.6:c.879G= MANE Select	NP_056446.4:p.Gln293=
ENST00000371217.10:c.879G= MANE Select	ENSP00000360261.5:p.Gln293=
NM_001143973.1:c.642G=	NP_001137445.1:p.Gln214=
NM_001143973.2:c.642G=	NP_001137445.1:p.Gln214=
NM_015631.5:c.879G=	NP_056446.4:p.Gln293=
ENST00000265993.13:c.933G=	ENSP00000265993.9:p.Gln311=
ENST00000371209.5:c.879G=	ENSP00000360253.5:p.Gln293=
ENST00000371217.9:c.879G=	ENSP00000360261.5:p.Gln293=
ENST00000430368.6:c.642G=	ENSP00000387567.1:p.Gln214=
ENST00000614499.4:c.879G=	ENSP00000483364.1:p.Gln293=
ENST00000614499.5:c.933G=	ENSP00000483364.2:p.Gln311=
ENST00000679485.1:n.903G=
ENST00000679566.1:c.852+540G=	ENSP00000505964.1:n.852+540G=
ENST00000679984.1:c.*134G=	ENSP00000504998.1:n.*134G=
ENST00000680144.1:c.879G=	ENSP00000506398.1:p.Gln293=
ENST00000680353.1:c.879G=	ENSP00000505367.1:p.Gln293=
ENST00000680697.1:n.543-1880G=
ENST00000680709.1:c.642G=	ENSP00000505830.1:p.Gln214=
ENST00000681127.1:n.932G=
ENST00000681739.1:n.934G=
ENST00000681928.1:c.*130+540G=	ENSP00000505552.1:n.*130+540G=
XM_005269690.1:c.933G=	XP_005269747.1:p.Gln311=
XM_005269690.2:c.933G=	XP_005269747.1:p.Gln311=
XM_011539627.1:c.933G=	XP_011537929.1:p.Gln311=
XM_011539627.2:c.933G=	XP_011537929.1:p.Gln311=
XM_011539628.1:c.933G=	XP_011537930.1:p.Gln311=
XM_011539628.2:c.933G=	XP_011537930.1:p.Gln311=
XM_024447935.1:c.933G=	XP_024303703.1:p.Gln311=