Canonical Allele Identifier: CA471020898

Gene: TCTN3

Linked Data

• dbSNP Id: rs2097948440
• gnomAD v4: 10-95686507-T-G
• MyVariant Identifiers: chr10:g.97446264T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686507T>G , CM000672.2:g.95686507T>G	GRCh38
NC_000010.10:g.97446264T>G , CM000672.1:g.97446264T>G	GRCh37
NC_000010.9:g.97436254T>G	NCBI36
NG_032953.1:g.12637A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.876A>C MANE Select	ENSP00000360261.5:p.Pro292=
ENST00000614499.5:c.930A>C	ENSP00000483364.2:p.Pro310=
ENST00000679485.1:n.900A>C
ENST00000679566.1:c.852+537A>C	ENSP00000505964.1:n.852+537A>C
ENST00000679984.1:c.*131A>C	ENSP00000504998.1:n.*131A>C
ENST00000680144.1:c.876A>C	ENSP00000506398.1:p.Pro292=
ENST00000680353.1:c.876A>C	ENSP00000505367.1:p.Pro292=
ENST00000680697.1:n.543-1883A>C
ENST00000680709.1:c.639A>C	ENSP00000505830.1:p.Pro213=
ENST00000681127.1:n.929A>C
ENST00000681739.1:n.931A>C
ENST00000681928.1:c.*130+537A>C	ENSP00000505552.1:n.*130+537A>C
ENST00000265993.13:c.930A>C	ENSP00000265993.9:p.Pro310=
ENST00000371209.5:c.876A>C	ENSP00000360253.5:p.Pro292=
ENST00000371217.9:c.876A>C	ENSP00000360261.5:p.Pro292=
ENST00000430368.6:c.639A>C	ENSP00000387567.1:p.Pro213=
ENST00000614499.4:c.876A>C	ENSP00000483364.1:p.Pro292=
NM_001143973.1:c.639A>C	NP_001137445.1:p.Pro213=
NM_015631.5:c.876A>C	NP_056446.4:p.Pro292=
XM_005269690.1:c.930A>C	XP_005269747.1:p.Pro310=
XM_011539627.1:c.930A>C	XP_011537929.1:p.Pro310=
XM_011539628.1:c.930A>C	XP_011537930.1:p.Pro310=
XM_005269690.2:c.930A>C	XP_005269747.1:p.Pro310=
XM_011539627.2:c.930A>C	XP_011537929.1:p.Pro310=
XM_011539628.2:c.930A>C	XP_011537930.1:p.Pro310=
XM_024447935.1:c.930A>C	XP_024303703.1:p.Pro310=
NM_015631.6:c.876A>C MANE Select	NP_056446.4:p.Pro292=
NM_001143973.2:c.639A>C	NP_001137445.1:p.Pro213=