Canonical Allele Identifier: CA354604766

Gene: TF

Linked Data

• gnomAD v4: 3-133756873-T-C
• MyVariant Identifiers: chr3:g.133475717T>C (hg19) ; chr3:g.133756873T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756873T>C , CM000665.2:g.133756873T>C	GRCh38
NC_000003.11:g.133475717T>C , CM000665.1:g.133475717T>C	GRCh37
NC_000003.10:g.134958407T>C	NCBI36
NG_013080.1:g.15741T>C
NG_013080.2:g.99876T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.734T>C MANE Select	ENSP00000385834.3:p.Leu245Pro
ENST00000402696.7:c.734T>C	ENSP00000385834.3:p.Leu245Pro
ENST00000482271.5:c.353T>C	ENSP00000419338.1:p.Leu118Pro
ENST00000485977.1:c.158-59T>C	ENSP00000418716.1:n.158-59T>C
NM_001063.3:c.734T>C	NP_001054.1:p.Leu245Pro
XM_011513100.1:c.734T>C	XP_011511402.1:p.Leu245Pro
NM_001354703.1:c.602T>C	NP_001341632.1:p.Leu201Pro
NM_001354704.1:c.353T>C	NP_001341633.1:p.Leu118Pro
NM_001063.4:c.734T>C MANE Select	NP_001054.2:p.Leu245Pro
NM_001354703.2:c.602T>C	NP_001341632.2:p.Leu201Pro
NM_001354704.2:c.353T>C	NP_001341633.2:p.Leu118Pro