Canonical Allele Identifier: CA11121078

Gene: TSGA10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.99154809C>T , CM000664.2:g.99154809C>T	GRCh38
NC_000002.11:g.99771272C>T , CM000664.1:g.99771272C>T	GRCh37
NC_000002.10:g.99137704C>T	NCBI36
NG_050665.1:g.4855C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025244.4:c.-737G>A MANE Select	NP_079520.1:n.-737G>A
ENST00000393483.8:c.-737G>A MANE Select	ENSP00000377123.3:n.-737G>A
NM_001349013.1:c.-635G>A	NP_001335942.1:n.-635G>A
NM_001349013.2:c.-635G>A	NP_001335942.1:n.-635G>A
NM_025244.3:c.-737G>A	NP_079520.1:n.-737G>A
NR_146053.1:n.158G>A
NR_146053.2:n.134G>A
NR_146054.1:n.130+28G>A
NR_146055.1:n.158G>A
NR_146055.2:n.134G>A
ENST00000393483.7:c.-737G>A	ENSP00000377123.3:n.-737G>A
ENST00000424491.5:c.63+4290C>T	ENSP00000390891.1:n.63+4290C>T
ENST00000465216.1:n.82G>A
ENST00000471174.5:n.154G>A
ENST00000476849.5:n.156G>A
ENST00000483914.5:n.33+28G>A
ENST00000489348.1:n.53G>A
XM_006712781.2:c.-722+28G>A	XP_006712844.1:n.-722+28G>A
XM_011511937.1:c.-529+28G>A	XP_011510239.1:n.-529+28G>A
XM_017005040.2:c.-806G>A	XP_016860529.1:n.-806G>A
XM_017005044.1:c.-690+28G>A	XP_016860533.1:n.-690+28G>A
XM_017005047.1:c.-516G>A	XP_016860536.1:n.-516G>A