Canonical Allele Identifier: CA3984320

Gene: TRDN

Linked Data

• ClinVar Variation Id: 506596
• ClinVar RCV Id: RCV000615338 ; RCV002531156 ; RCV002498899
• dbSNP Id: rs142018848
• ExAC: 6:123825065 T / A
• gnomAD v2: 6-123825065-T-A
• gnomAD v3: 6-123503920-T-A
• gnomAD v4: 6-123503920-T-A
• MyVariant Identifiers: chr6:g.123825065T>A (hg19) ; chr6:g.123503920T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.123503920T>A , CM000668.2:g.123503920T>A	GRCh38
NC_000006.11:g.123825065T>A , CM000668.1:g.123825065T>A	GRCh37
NC_000006.10:g.123866764T>A	NCBI36
NG_030438.1:g.138174A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361029.9:c.413-19A>T	ENSP00000354307.5:n.413-19A>T
ENST00000546248.6:c.611-19A>T	ENSP00000439281.2:n.611-19A>T
ENST00000334268.9:c.611-19A>T MANE Select	ENSP00000333984.5:n.611-19A>T
ENST00000662930.1:c.611-19A>T	ENSP00000499585.1:n.611-19A>T
ENST00000334268.8:c.611-19A>T	ENSP00000333984.5:n.611-19A>T
ENST00000361029.8:c.127-19A>T
ENST00000546248.5:c.611-19A>T	ENSP00000439281.2:n.611-19A>T
ENST00000628709.2:c.611-19A>T	ENSP00000486095.1:n.611-19A>T
NM_001251987.1:c.611-19A>T	NP_001238916.1:n.611-19A>T
NM_001256020.1:c.611-19A>T	NP_001242949.1:n.611-19A>T
NM_001256021.1:c.611-19A>T	NP_001242950.1:n.611-19A>T
NM_006073.3:c.611-19A>T	NP_006064.2:n.611-19A>T
XM_011535382.1:c.611-19A>T	XP_011533684.1:n.611-19A>T
NM_006073.4:c.611-19A>T MANE Select	NP_006064.2:n.611-19A>T
NM_001251987.2:c.611-19A>T	NP_001238916.1:n.611-19A>T
NM_001256020.2:c.611-19A>T	NP_001242949.1:n.611-19A>T
NM_001256021.2:c.611-19A>T	NP_001242950.1:n.611-19A>T