Canonical Allele Identifier: CA211804882

Gene: TCTN3

Linked Data

• dbSNP Id: rs571647979
• gnomAD v3: 10-95686604-C-G
• gnomAD v4: 10-95686604-C-G
• MyVariant Identifiers: chr10:g.97446361C>G (hg19) ; chr10:g.95686604C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686604C>G , CM000672.2:g.95686604C>G	GRCh38
NC_000010.10:g.97446361C>G , CM000672.1:g.97446361C>G	GRCh37
NC_000010.9:g.97436351C>G	NCBI36
NG_032953.1:g.12540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.853-74G>C MANE Select	ENSP00000360261.5:n.853-74G>C
ENST00000614499.5:c.907-74G>C	ENSP00000483364.2:n.907-74G>C
ENST00000679485.1:n.877-74G>C
ENST00000679566.1:c.852+440G>C	ENSP00000505964.1:n.852+440G>C
ENST00000679984.1:c.*108-74G>C	ENSP00000504998.1:n.*108-74G>C
ENST00000680144.1:c.853-74G>C	ENSP00000506398.1:n.853-74G>C
ENST00000680353.1:c.853-74G>C	ENSP00000505367.1:n.853-74G>C
ENST00000680697.1:n.543-1980G>C
ENST00000680709.1:c.616-74G>C	ENSP00000505830.1:n.616-74G>C
ENST00000681127.1:n.906-74G>C
ENST00000681739.1:n.908-74G>C
ENST00000681928.1:c.*130+440G>C	ENSP00000505552.1:n.*130+440G>C
ENST00000265993.13:c.907-74G>C	ENSP00000265993.9:n.907-74G>C
ENST00000371209.5:c.853-74G>C	ENSP00000360253.5:n.853-74G>C
ENST00000371217.9:c.853-74G>C	ENSP00000360261.5:n.853-74G>C
ENST00000430368.6:c.616-74G>C	ENSP00000387567.1:n.616-74G>C
ENST00000614499.4:c.853-74G>C	ENSP00000483364.1:n.853-74G>C
NM_001143973.1:c.616-74G>C	NP_001137445.1:n.616-74G>C
NM_015631.5:c.853-74G>C	NP_056446.4:n.853-74G>C
XM_005269690.1:c.907-74G>C	XP_005269747.1:n.907-74G>C
XM_011539627.1:c.907-74G>C	XP_011537929.1:n.907-74G>C
XM_011539628.1:c.907-74G>C	XP_011537930.1:n.907-74G>C
XM_005269690.2:c.907-74G>C	XP_005269747.1:n.907-74G>C
XM_011539627.2:c.907-74G>C	XP_011537929.1:n.907-74G>C
XM_011539628.2:c.907-74G>C	XP_011537930.1:n.907-74G>C
XM_024447935.1:c.907-74G>C	XP_024303703.1:n.907-74G>C
NM_015631.6:c.853-74G>C MANE Select	NP_056446.4:n.853-74G>C
NM_001143973.2:c.616-74G>C	NP_001137445.1:n.616-74G>C