Canonical Allele Identifier: CA272036824

Gene: TPM1

Linked Data

• dbSNP Id: rs1005599559
• gnomAD v3: 15-63066184-G-T
• gnomAD v4: 15-63066184-G-T
• MyVariant Identifiers: chr15:g.63358383G>T (hg19) ; chr15:g.63066184G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.63066184G>T , CM000677.2:g.63066184G>T	GRCh38
NC_000015.9:g.63358383G>T , CM000677.1:g.63358383G>T	GRCh37
NC_000015.8:g.61145436G>T	NCBI36
NG_007557.1:g.28546G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558868.6:n.1555+3539G>T
ENST00000559831.6:c.*191+3539G>T	ENSP00000452977.2:n.*191+3539G>T
ENST00000560615.6:c.394+3539G>T	ENSP00000453050.2:n.394+3539G>T
ENST00000651622.2:c.*1026+99G>T	ENSP00000498540.2:n.*1026+99G>T
ENST00000705544.1:c.728+99G>T
ENST00000317516.12:c.664+3539G>T	ENSP00000322577.7:n.664+3539G>T
ENST00000334895.10:c.664+3539G>T	ENSP00000334624.4:n.664+3539G>T
ENST00000357980.9:c.898+3539G>T	ENSP00000350667.4:n.898+3539G>T
ENST00000404484.9:c.664+3539G>T	ENSP00000384315.4:n.664+3539G>T
ENST00000559397.6:c.772+3539G>T	ENSP00000452879.1:n.772+3539G>T
ENST00000644204.1:n.794+3539G>T
ENST00000651344.1:n.1288+3539G>T
ENST00000651577.1:c.394+3539G>T	ENSP00000498730.1:n.394+3539G>T
ENST00000651590.1:c.*98+99G>T	ENSP00000498284.1:n.*98+99G>T
ENST00000651704.1:c.394+3539G>T	ENSP00000498562.1:n.394+3539G>T
ENST00000267996.11:c.772+3539G>T	ENSP00000267996.7:n.772+3539G>T
ENST00000317516.11:c.664+3539G>T	ENSP00000322577.7:n.664+3539G>T
ENST00000334895.9:c.664+3539G>T	ENSP00000334624.4:n.664+3539G>T
ENST00000357980.8:c.898+3539G>T	ENSP00000350667.4:n.898+3539G>T
ENST00000358278.7:c.772+3539G>T	ENSP00000351022.3:n.772+3539G>T
ENST00000404484.8:c.664+3539G>T	ENSP00000384315.4:n.664+3539G>T
ENST00000558072.5:n.291+3539G>T
ENST00000558264.5:c.*191+3539G>T	ENSP00000452624.1:n.*191+3539G>T
ENST00000558347.5:c.*180+3539G>T	ENSP00000452887.1:n.*180+3539G>T
ENST00000558544.5:c.*380+3539G>T	ENSP00000453817.1:n.*380+3539G>T
ENST00000559397.5:c.772+3539G>T	ENSP00000452879.1:n.772+3539G>T
ENST00000559556.5:c.772+3539G>T	ENSP00000453941.1:n.772+3539G>T
ENST00000560975.5:n.2621+3539G>T
NM_001018004.1:c.772+3539G>T	NP_001018004.1:n.772+3539G>T
NM_001018006.1:c.772+3539G>T	NP_001018006.1:n.772+3539G>T
NM_001018007.1:c.772+3539G>T	NP_001018007.1:n.772+3539G>T
NM_001018008.1:c.664+3539G>T	NP_001018008.1:n.664+3539G>T
NM_001018020.1:c.772+3539G>T	NP_001018020.1:n.772+3539G>T
NM_001301289.1:c.664+3539G>T	NP_001288218.1:n.664+3539G>T
XM_005254637.1:c.898+3539G>T	XP_005254694.1:n.898+3539G>T
XM_005254645.1:c.772+3539G>T	XP_005254702.1:n.772+3539G>T
XM_005254652.1:c.664+3539G>T	XP_005254709.1:n.664+3539G>T
XM_005254653.1:c.664+3539G>T	XP_005254710.1:n.664+3539G>T
NM_001330344.1:c.664+3539G>T	NP_001317273.1:n.664+3539G>T
NM_001330351.1:c.664+3539G>T	NP_001317280.1:n.664+3539G>T
NM_001365776.1:c.772+3539G>T	NP_001352705.1:n.772+3539G>T
NM_001365778.1:c.898+3539G>T	NP_001352707.1:n.898+3539G>T
XM_017022539.2:c.772+3539G>T	XP_016878028.2:n.772+3539G>T
XR_002957675.1:n.1730+3539G>T
NM_001018004.2:c.772+3539G>T	NP_001018004.1:n.772+3539G>T
NM_001018006.2:c.772+3539G>T	NP_001018006.1:n.772+3539G>T
NM_001018007.2:c.772+3539G>T	NP_001018007.1:n.772+3539G>T
NM_001018008.2:c.664+3539G>T	NP_001018008.1:n.664+3539G>T
NM_001018020.2:c.772+3539G>T	NP_001018020.1:n.772+3539G>T
NM_001301289.2:c.664+3539G>T	NP_001288218.1:n.664+3539G>T
NM_001330344.2:c.664+3539G>T	NP_001317273.1:n.664+3539G>T
NM_001330351.2:c.664+3539G>T	NP_001317280.1:n.664+3539G>T