Canonical Allele Identifier: CA600238677

Gene: TCIRG1

Linked Data

• dbSNP Id: rs1477946543
• gnomAD v2: 11-67816198-CTGT-C
• gnomAD v3: 11-68048731-CTGT-C
• gnomAD v4: 11-68048731-CTGT-C
• MyVariant Identifiers: chr11:g.67816199_67816201del (hg19) ; chr11:g.68048732_68048734del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048734_68048736del , CM000673.2:g.68048734_68048736del	GRCh38
NC_000011.9:g.67816201_67816203del , CM000673.1:g.67816201_67816203del	GRCh37
NC_000011.8:g.67572777_67572779del	NCBI36
NG_007878.1:g.14719_14721del , LRG_115:g.14719_14721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.180-145_180-143del
ENST00000698254.1:c.1084-145_1084-143del	ENSP00000513629.1:n.1084-145_1084-143del
ENST00000698255.1:c.1504-145_1504-143del	ENSP00000513630.1:n.1504-145_1504-143del
ENST00000698256.1:c.1021-145_1021-143del
ENST00000698257.1:n.973-145_973-143del
ENST00000698258.1:n.690-145_690-143del
ENST00000698259.1:n.456-145_456-143del
ENST00000265686.8:c.1555-145_1555-143del MANE Select	ENSP00000265686.3:n.1555-145_1555-143del
ENST00000265686.7:c.1555-145_1555-143del	ENSP00000265686.3:n.1555-145_1555-143del
ENST00000525724.5:n.867-145_867-143del
ENST00000528981.5:c.707-145_707-143del
ENST00000532635.5:c.907-145_907-143del	ENSP00000434407.1:n.907-145_907-143del
ENST00000533005.5:n.668-145_668-143del
NM_006019.3:c.1555-145_1555-143del	NP_006010.2:n.1555-145_1555-143del
NM_006053.3:c.907-145_907-143del	NP_006044.1:n.907-145_907-143del
XM_005273709.2:c.1555-145_1555-143del	XP_005273766.1:n.1555-145_1555-143del
XM_011544726.1:c.1555-145_1555-143del	XP_011543028.1:n.1555-145_1555-143del
XM_011544727.1:c.1555-145_1555-143del	XP_011543029.1:n.1555-145_1555-143del
XM_011544728.1:c.1555-145_1555-143del	XP_011543030.1:n.1555-145_1555-143del
XR_949754.1:n.1559-145_1559-143del
NM_001351059.1:c.661-145_661-143del	NP_001337988.1:n.661-145_661-143del
XM_024448320.1:c.1648-145_1648-143del	XP_024304088.1:n.1648-145_1648-143del
XM_024448321.1:c.1648-145_1648-143del	XP_024304089.1:n.1648-145_1648-143del
XM_024448322.1:c.1648-145_1648-143del	XP_024304090.1:n.1648-145_1648-143del
XM_024448323.1:c.1648-145_1648-143del	XP_024304091.1:n.1648-145_1648-143del
XM_024448324.1:c.1648-145_1648-143del	XP_024304092.1:n.1648-145_1648-143del
XR_001747721.2:n.1679-145_1679-143del
XR_001747722.1:n.1692-145_1692-143del
XR_001747723.2:n.1692-145_1692-143del
XR_002957115.1:n.1770-145_1770-143del
NM_006019.4:c.1555-145_1555-143del MANE Select	NP_006010.2:n.1555-145_1555-143del
NM_001351059.2:c.661-145_661-143del	NP_001337988.1:n.661-145_661-143del
NM_006053.4:c.907-145_907-143del	NP_006044.1:n.907-145_907-143del