Canonical Allele Identifier: CA2182486096

Gene: TPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63042689G= , CM000677.2:g.63042689G=	GRCh38
NC_000015.9:g.63334888G= , CM000677.1:g.63334888G=	GRCh37
NC_000015.8:g.61121941G=	NCBI36
NG_007557.1:g.5051G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559831.6:c.-141G=	ENSP00000452977.2:n.-141G=
ENST00000651344.1:n.42G=
ENST00000288398.10:c.-141G=	ENSP00000288398.6:n.-141G=
ENST00000358278.7:c.-141G=	ENSP00000351022.3:n.-141G=
ENST00000560975.5:n.6G=
ENST00000610733.1:c.-141G=	ENSP00000477929.1:n.-141G=
NM_000366.5:c.-141G=	NP_000357.3:n.-141G=
NM_001018004.1:c.-141G=	NP_001018004.1:n.-141G=
NM_001018005.1:c.-141G=	NP_001018005.1:n.-141G=
NM_001018006.1:c.-141G=	NP_001018006.1:n.-141G=
NM_001018007.1:c.-141G=	NP_001018007.1:n.-141G=
NM_001018020.1:c.-141G=	NP_001018020.1:n.-141G=
NM_001301244.1:c.-141G=	NP_001288173.1:n.-141G=
XM_005254637.1:c.-141G=	XP_005254694.1:n.-141G=
XM_005254638.2:c.-141G=	XP_005254695.1:n.-141G=
XM_005254639.2:c.-141G=	XP_005254696.1:n.-141G=
XM_005254640.2:c.-141G=	XP_005254697.1:n.-141G=
XM_005254641.2:c.-141G=	XP_005254698.1:n.-141G=
XM_005254645.1:c.-141G=	XP_005254702.1:n.-141G=
XM_006720667.2:c.-141G=	XP_006720730.1:n.-141G=