Canonical Allele Identifier: CA993986060
Gene: TPM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090388058

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.16074810A>G , CM000681.2:g.16074810A>G GRCh38
NC_000019.9:g.16185620A>G , CM000681.1:g.16185620A>G GRCh37
NC_000019.8:g.16046620A>G NCBI36
NG_015841.1:g.12304A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000586499.6:c.264-1237A>G ENSP00000468246.2:n.264-1237A>G
ENST00000646974.2:c.115-1237A>G ENSP00000494125.1:n.115-1237A>G
ENST00000647464.2:c.7-1237A>G ENSP00000496648.2:n.7-1237A>G
ENST00000344824.10:c.115-1237A>G ENSP00000345230.5:n.115-1237A>G
ENST00000586499.5:c.67-1237A>G ENSP00000468246.1:n.67-1237A>G
ENST00000589897.1:c.115-1237A>G ENSP00000466158.1:n.115-1237A>G
NM_001145160.1:c.115-1237A>G NP_001138632.1:n.115-1237A>G
XM_006722865.1:c.115-1237A>G XP_006722928.1:n.115-1237A>G
XM_006722865.2:c.115-1237A>G XP_006722928.1:n.115-1237A>G
XM_017027188.1:c.67-1237A>G XP_016882677.1:n.67-1237A>G
NM_001145160.2:c.115-1237A>G NP_001138632.1:n.115-1237A>G
NM_001367836.1:c.67-1237A>G NP_001354765.1:n.67-1237A>G