Canonical Allele Identifier: CA600238420
Gene: TCIRG1 HGNC NCBI

Linked Data

dbSNP Id: rs1358861198

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047926dup , CM000673.2:g.68047926dup GRCh38
NC_000011.9:g.67815393dup , CM000673.1:g.67815393dup GRCh37
NC_000011.8:g.67571969dup NCBI36
NG_007878.1:g.13911dup , LRG_115:g.13911dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.133dup
ENST00000698254.1:c.1037dup ENSP00000513629.1:p.Asn346LysfsTer?
ENST00000698255.1:c.1457dup ENSP00000513630.1:p.Asn486LysfsTer?
ENST00000698256.1:c.974dup
ENST00000698257.1:n.926dup
ENST00000698258.1:n.643dup
ENST00000698259.1:n.409dup
ENST00000265686.8:c.1508dup MANE Select ENSP00000265686.3:p.Asn503LysfsTer?
ENST00000265686.7:c.1508dup ENSP00000265686.3:p.Asn503LysfsTer?
ENST00000525516.1:n.302dup
ENST00000525724.5:n.820dup
ENST00000528981.5:c.660dup
ENST00000532635.5:c.860dup ENSP00000434407.1:p.Asn287LysfsTer?
ENST00000533005.5:n.621dup
NM_006019.3:c.1508dup NP_006010.2:p.Asn503LysfsTer?
NM_006053.3:c.860dup NP_006044.1:p.Asn287LysfsTer?
XM_005273709.2:c.1508dup XP_005273766.1:p.Asn503LysfsTer?
XM_011544726.1:c.1508dup XP_011543028.1:p.Asn503LysfsTer?
XM_011544727.1:c.1508dup XP_011543029.1:p.Asn503LysfsTer?
XM_011544728.1:c.1508dup XP_011543030.1:p.Asn503LysfsTer?
XR_949754.1:n.1512dup
NM_001351059.1:c.614dup NP_001337988.1:p.Asn205LysfsTer?
XM_024448320.1:c.1601dup XP_024304088.1:p.Asn534LysfsTer?
XM_024448321.1:c.1601dup XP_024304089.1:p.Asn534LysfsTer?
XM_024448322.1:c.1601dup XP_024304090.1:p.Asn534LysfsTer?
XM_024448323.1:c.1601dup XP_024304091.1:p.Asn534LysfsTer?
XM_024448324.1:c.1601dup XP_024304092.1:p.Asn534LysfsTer?
XR_001747721.2:n.1632dup
XR_001747722.1:n.1645dup
XR_001747723.2:n.1645dup
XR_002957115.1:n.1723dup
NM_006019.4:c.1508dup MANE Select NP_006010.2:p.Asn503LysfsTer?
NM_001351059.2:c.614dup NP_001337988.1:p.Asn205LysfsTer?
NM_006053.4:c.860dup NP_006044.1:p.Asn287LysfsTer?