Canonical Allele Identifier: CA600238440

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1373523711
• gnomAD v2: 11-67815252-GCCAACC-G
• gnomAD v3: 11-68047785-GCCAACC-G
• gnomAD v4: 11-68047785-GCCAACC-G
• MyVariant Identifiers: chr11:g.67815253_67815258del (hg19) ; chr11:g.68047786_68047791del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68047786_68047791del , CM000673.2:g.68047786_68047791del	GRCh38
NC_000011.9:g.67815253_67815258del , CM000673.1:g.67815253_67815258del	GRCh37
NC_000011.8:g.67571829_67571834del	NCBI36
NG_007878.1:g.13771_13776del , LRG_115:g.13771_13776del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.70_75del
ENST00000698254.1:c.974_979del	ENSP00000513629.1:p.Ala325_Gln327delinsGlu
ENST00000698255.1:c.1394_1399del	ENSP00000513630.1:p.Ala465_Gln467delinsGlu
ENST00000698256.1:c.911_916del
ENST00000698257.1:n.863_868del
ENST00000698258.1:n.503_508del
ENST00000698259.1:n.269_274del
ENST00000265686.8:c.1445_1450del MANE Select	ENSP00000265686.3:p.Ala482_Gln484delinsGlu
ENST00000265686.7:c.1445_1450del	ENSP00000265686.3:p.Ala482_Gln484delinsGlu
ENST00000525516.1:n.239_244del
ENST00000525724.5:n.757_762del
ENST00000528981.5:c.597_602del
ENST00000529364.1:c.856_861del
ENST00000532635.5:c.797_802del	ENSP00000434407.1:p.Ala266_Gln268delinsGlu
ENST00000533005.5:n.481_486del
NM_006019.3:c.1445_1450del	NP_006010.2:p.Ala482_Gln484delinsGlu
NM_006053.3:c.797_802del	NP_006044.1:p.Ala266_Gln268delinsGlu
XM_005273709.2:c.1445_1450del	XP_005273766.1:p.Ala482_Gln484delinsGlu
XM_011544726.1:c.1445_1450del	XP_011543028.1:p.Ala482_Gln484delinsGlu
XM_011544727.1:c.1445_1450del	XP_011543029.1:p.Ala482_Gln484delinsGlu
XM_011544728.1:c.1445_1450del	XP_011543030.1:p.Ala482_Gln484delinsGlu
XM_011544729.1:c.1461_1466del	XP_011543031.1:p.Gln488_Pro489del
XR_949754.1:n.1449_1454del
NM_001351059.1:c.551_556del	NP_001337988.1:p.Ala184_Gln186delinsGlu
XM_024448320.1:c.1461_1466del	XP_024304088.1:p.Gln488_Pro489del
XM_024448321.1:c.1461_1466del	XP_024304089.1:p.Gln488_Pro489del
XM_024448322.1:c.1461_1466del	XP_024304090.1:p.Gln488_Pro489del
XM_024448323.1:c.1461_1466del	XP_024304091.1:p.Gln488_Pro489del
XM_024448324.1:c.1461_1466del	XP_024304092.1:p.Gln488_Pro489del
XR_001747721.2:n.1569_1574del
XR_001747722.1:n.1582_1587del
XR_001747723.2:n.1582_1587del
XR_002957115.1:n.1583_1588del
NM_006019.4:c.1445_1450del MANE Select	NP_006010.2:p.Ala482_Gln484delinsGlu
NM_001351059.2:c.551_556del	NP_001337988.1:p.Ala184_Gln186delinsGlu
NM_006053.4:c.797_802del	NP_006044.1:p.Ala266_Gln268delinsGlu