Canonical Allele Identifier: CA305887435

Gene: TPM4

Linked Data

• dbSNP Id: rs753102704
• gnomAD v2: 19-16185568-G-A
• gnomAD v3: 19-16074758-G-A
• gnomAD v4: 19-16074758-G-A
• MyVariant Identifiers: chr19:g.16185568G>A (hg19) ; chr19:g.16074758G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16074758G>A , CM000681.2:g.16074758G>A	GRCh38
NC_000019.9:g.16185568G>A , CM000681.1:g.16185568G>A	GRCh37
NC_000019.8:g.16046568G>A	NCBI36
NG_015841.1:g.12252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586499.6:c.264-1289G>A	ENSP00000468246.2:n.264-1289G>A
ENST00000646974.2:c.115-1289G>A	ENSP00000494125.1:n.115-1289G>A
ENST00000647464.2:c.7-1289G>A	ENSP00000496648.2:n.7-1289G>A
ENST00000344824.10:c.115-1289G>A	ENSP00000345230.5:n.115-1289G>A
ENST00000586499.5:c.67-1289G>A	ENSP00000468246.1:n.67-1289G>A
ENST00000589897.1:c.115-1289G>A	ENSP00000466158.1:n.115-1289G>A
NM_001145160.1:c.115-1289G>A	NP_001138632.1:n.115-1289G>A
XM_006722865.1:c.115-1289G>A	XP_006722928.1:n.115-1289G>A
XM_006722865.2:c.115-1289G>A	XP_006722928.1:n.115-1289G>A
XM_017027188.1:c.67-1289G>A	XP_016882677.1:n.67-1289G>A
NM_001145160.2:c.115-1289G>A	NP_001138632.1:n.115-1289G>A
NM_001367836.1:c.67-1289G>A	NP_001354765.1:n.67-1289G>A