Canonical Allele Identifier: CA12320550

Gene: TCF19 POU5F1

Linked Data

• dbSNP Id: rs3130931
• gnomAD v2: 6-31134888-T-C
• gnomAD v3: 6-31167111-T-C
• gnomAD v4: 6-31167111-T-C
• MyVariant Identifiers: chr6:g.31134888T>C (hg19) ; chr6:g.31167111T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31167111T>C , CM000668.2:g.31167111T>C	GRCh38
NC_000006.11:g.31134888T>C , CM000668.1:g.31134888T>C	GRCh37
NC_000006.10:g.31242867T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000542218.2:c.*103T>C (TCF19)	ENSP00000439397.2:n.*103T>C
ENST00000259915.13:c.406-1064A>G (POU5F1) MANE Select	ENSP00000259915.7:n.406-1064A>G
ENST00000259915.12:c.406-1064A>G (POU5F1)	ENSP00000259915.7:n.406-1064A>G
ENST00000441888.7:c.-183-1064A>G (POU5F1)	ENSP00000389359.2:n.-183-1064A>G
ENST00000461401.1:n.444-1064A>G (POU5F1)
ENST00000513407.1:c.-1472A>G (POU5F1)	ENSP00000475512.1:n.-1472A>G
ENST00000542218.1:c.757T>C (TCF19)	ENSP00000439397.1:n.757T>C
ENST00000619340.1:c.406-1064A>G (POU5F1)	ENSP00000481679.1:n.406-1064A>G
ENST00000620031.4:c.-683A>G (POU5F1)	ENSP00000484778.1:n.-683A>G
NM_001173531.2:c.-683A>G (POU5F1)	NP_001167002.1:n.-683A>G
NM_001285986.1:c.-1472A>G (POU5F1)	NP_001272915.1:n.-1472A>G
NM_001285987.1:c.-944A>G (POU5F1)	NP_001272916.1:n.-944A>G
NM_002701.5:c.406-1064A>G (POU5F1)	NP_002692.2:n.406-1064A>G
NM_203289.5:c.-1169A>G (POU5F1)	NP_976034.4:n.-1169A>G
NM_002701.6:c.406-1064A>G (POU5F1) MANE Select	NP_002692.2:n.406-1064A>G
NM_001173531.3:c.-683A>G (POU5F1)	NP_001167002.1:n.-683A>G
NM_001285986.2:c.-1472A>G (POU5F1)	NP_001272915.1:n.-1472A>G
NM_203289.6:c.-1169A>G (POU5F1)	NP_976034.4:n.-1169A>G