Canonical Allele Identifier: CA2325194820
Gene: TPM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.16074808C= , CM000681.2:g.16074808C= GRCh38
NC_000019.9:g.16185618C= , CM000681.1:g.16185618C= GRCh37
NC_000019.8:g.16046618C= NCBI36
NG_015841.1:g.12302C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000586499.6:c.264-1239C= ENSP00000468246.2:n.264-1239C=
ENST00000646974.2:c.115-1239C= ENSP00000494125.1:n.115-1239C=
ENST00000647464.2:c.7-1239C= ENSP00000496648.2:n.7-1239C=
ENST00000344824.10:c.115-1239C= ENSP00000345230.5:n.115-1239C=
ENST00000586499.5:c.67-1239C= ENSP00000468246.1:n.67-1239C=
ENST00000589897.1:c.115-1239C= ENSP00000466158.1:n.115-1239C=
NM_001145160.1:c.115-1239C= NP_001138632.1:n.115-1239C=
XM_006722865.1:c.115-1239C= XP_006722928.1:n.115-1239C=
XM_006722865.2:c.115-1239C= XP_006722928.1:n.115-1239C=
XM_017027188.1:c.67-1239C= XP_016882677.1:n.67-1239C=
NM_001145160.2:c.115-1239C= NP_001138632.1:n.115-1239C=
NM_001367836.1:c.67-1239C= NP_001354765.1:n.67-1239C=