Canonical Allele Identifier: CA595349968

Gene: TCTN3

Linked Data

• dbSNP Id: rs1286136095
• gnomAD v2: 10-97446294-G-A
• gnomAD v4: 10-95686537-G-A
• MyVariant Identifiers: chr10:g.97446294G>A (hg19) ; chr10:g.95686537G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95686537G>A , CM000672.2:g.95686537G>A	GRCh38
NC_000010.10:g.97446294G>A , CM000672.1:g.97446294G>A	GRCh37
NC_000010.9:g.97436284G>A	NCBI36
NG_032953.1:g.12607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371217.10:c.853-7C>T MANE Select	ENSP00000360261.5:n.853-7C>T
ENST00000614499.5:c.907-7C>T	ENSP00000483364.2:n.907-7C>T
ENST00000679485.1:n.877-7C>T
ENST00000679566.1:c.852+507C>T	ENSP00000505964.1:n.852+507C>T
ENST00000679984.1:c.*108-7C>T	ENSP00000504998.1:n.*108-7C>T
ENST00000680144.1:c.853-7C>T	ENSP00000506398.1:n.853-7C>T
ENST00000680353.1:c.853-7C>T	ENSP00000505367.1:n.853-7C>T
ENST00000680697.1:n.543-1913C>T
ENST00000680709.1:c.616-7C>T	ENSP00000505830.1:n.616-7C>T
ENST00000681127.1:n.906-7C>T
ENST00000681739.1:n.908-7C>T
ENST00000681928.1:c.*130+507C>T	ENSP00000505552.1:n.*130+507C>T
ENST00000265993.13:c.907-7C>T	ENSP00000265993.9:n.907-7C>T
ENST00000371209.5:c.853-7C>T	ENSP00000360253.5:n.853-7C>T
ENST00000371217.9:c.853-7C>T	ENSP00000360261.5:n.853-7C>T
ENST00000430368.6:c.616-7C>T	ENSP00000387567.1:n.616-7C>T
ENST00000614499.4:c.853-7C>T	ENSP00000483364.1:n.853-7C>T
NM_001143973.1:c.616-7C>T	NP_001137445.1:n.616-7C>T
NM_015631.5:c.853-7C>T	NP_056446.4:n.853-7C>T
XM_005269690.1:c.907-7C>T	XP_005269747.1:n.907-7C>T
XM_011539627.1:c.907-7C>T	XP_011537929.1:n.907-7C>T
XM_011539628.1:c.907-7C>T	XP_011537930.1:n.907-7C>T
XM_005269690.2:c.907-7C>T	XP_005269747.1:n.907-7C>T
XM_011539627.2:c.907-7C>T	XP_011537929.1:n.907-7C>T
XM_011539628.2:c.907-7C>T	XP_011537930.1:n.907-7C>T
XM_024447935.1:c.907-7C>T	XP_024303703.1:n.907-7C>T
NM_015631.6:c.853-7C>T MANE Select	NP_056446.4:n.853-7C>T
NM_001143973.2:c.616-7C>T	NP_001137445.1:n.616-7C>T