Canonical Allele Identifier: CA1746651485

Gene: TRIM24

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.138472645A>C , CM000669.2:g.138472645A>C	GRCh38
NC_000007.13:g.138157390A>C , CM000669.1:g.138157390A>C	GRCh37
NC_000007.12:g.137807930A>C	NCBI36
NG_023286.1:g.17312A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343526.9:c.364+11733A>C MANE Select	ENSP00000340507.4:n.364+11733A>C
ENST00000343526.8:c.364+11733A>C	ENSP00000340507.4:n.364+11733A>C
ENST00000415680.6:c.364+11733A>C	ENSP00000390829.2:n.364+11733A>C
ENST00000497516.5:n.238+11343A>C
ENST00000620194.1:c.352+11733A>C	ENSP00000484482.1:n.352+11733A>C
NM_003852.3:c.364+11733A>C	NP_003843.3:n.364+11733A>C
NM_015905.2:c.364+11733A>C	NP_056989.2:n.364+11733A>C
XM_011516650.1:c.364+11733A>C	XP_011514952.1:n.364+11733A>C
XM_024446981.1:c.307+11343A>C	XP_024302749.1:n.307+11343A>C
NM_015905.3:c.364+11733A>C MANE Select	NP_056989.2:n.364+11733A>C
NM_003852.4:c.364+11733A>C	NP_003843.3:n.364+11733A>C