Canonical Allele Identifier: CA2574899539

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047900_68047902del , CM000673.2:g.68047900_68047902del	GRCh38
NC_000011.9:g.67815367_67815369del , CM000673.1:g.67815367_67815369del	GRCh37
NC_000011.8:g.67571943_67571945del	NCBI36
NG_007878.1:g.13885_13887del , LRG_115:g.13885_13887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.107_109del
ENST00000698254.1:c.1011_1013del	ENSP00000513629.1:p.Gln337del
ENST00000698255.1:c.1431_1433del	ENSP00000513630.1:p.Gln477del
ENST00000698256.1:c.948_950del
ENST00000698257.1:n.900_902del
ENST00000698258.1:n.617_619del
ENST00000698259.1:n.383_385del
ENST00000265686.8:c.1482_1484del MANE Select	ENSP00000265686.3:p.Gln494del
ENST00000265686.7:c.1482_1484del	ENSP00000265686.3:p.Gln494del
ENST00000525516.1:n.276_278del
ENST00000525724.5:n.794_796del
ENST00000528981.5:c.634_636del
ENST00000532635.5:c.834_836del	ENSP00000434407.1:p.Gln278del
ENST00000533005.5:n.595_597del
NM_006019.3:c.1482_1484del	NP_006010.2:p.Gln494del
NM_006053.3:c.834_836del	NP_006044.1:p.Gln278del
XM_005273709.2:c.1482_1484del	XP_005273766.1:p.Gln494del
XM_011544726.1:c.1482_1484del	XP_011543028.1:p.Gln494del
XM_011544727.1:c.1482_1484del	XP_011543029.1:p.Gln494del
XM_011544728.1:c.1482_1484del	XP_011543030.1:p.Gln494del
XR_949754.1:n.1486_1488del
NM_001351059.1:c.588_590del	NP_001337988.1:p.Gln196del
XM_024448320.1:c.1575_1577del	XP_024304088.1:p.Gln525del
XM_024448321.1:c.1575_1577del	XP_024304089.1:p.Gln525del
XM_024448322.1:c.1575_1577del	XP_024304090.1:p.Gln525del
XM_024448323.1:c.1575_1577del	XP_024304091.1:p.Gln525del
XM_024448324.1:c.1575_1577del	XP_024304092.1:p.Gln525del
XR_001747721.2:n.1606_1608del
XR_001747722.1:n.1619_1621del
XR_001747723.2:n.1619_1621del
XR_002957115.1:n.1697_1699del
NM_006019.4:c.1482_1484del MANE Select	NP_006010.2:p.Gln494del
NM_001351059.2:c.588_590del	NP_001337988.1:p.Gln196del
NM_006053.4:c.834_836del	NP_006044.1:p.Gln278del