Canonical Allele Identifier: CA15947553
Gene: TPM4 HGNC NCBI

Linked Data

dbSNP Id: rs8109288
gnomAD v2: 19-16185559-G-A
gnomAD v3: 19-16074749-G-A
gnomAD v4: 19-16074749-G-A
MyVariant Identifiers: chr19:g.16185559G>A (hg19) chr19:g.16074749G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.16074749G>A , CM000681.2:g.16074749G>A GRCh38
NC_000019.9:g.16185559G>A , CM000681.1:g.16185559G>A GRCh37
NC_000019.8:g.16046559G>A NCBI36
NG_015841.1:g.12243G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000586499.6:c.264-1298G>A ENSP00000468246.2:n.264-1298G>A
ENST00000646974.2:c.115-1298G>A ENSP00000494125.1:n.115-1298G>A
ENST00000647464.2:c.7-1298G>A ENSP00000496648.2:n.7-1298G>A
ENST00000344824.10:c.115-1298G>A ENSP00000345230.5:n.115-1298G>A
ENST00000586499.5:c.67-1298G>A ENSP00000468246.1:n.67-1298G>A
ENST00000589897.1:c.115-1298G>A ENSP00000466158.1:n.115-1298G>A
NM_001145160.1:c.115-1298G>A NP_001138632.1:n.115-1298G>A
XM_006722865.1:c.115-1298G>A XP_006722928.1:n.115-1298G>A
XM_006722865.2:c.115-1298G>A XP_006722928.1:n.115-1298G>A
XM_017027188.1:c.67-1298G>A XP_016882677.1:n.67-1298G>A
NM_001145160.2:c.115-1298G>A NP_001138632.1:n.115-1298G>A
NM_001367836.1:c.67-1298G>A NP_001354765.1:n.67-1298G>A
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