Canonical Allele Identifier: CA1980431631

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048750_68048756delinsGGGTGAT , CM000673.2:g.68048750_68048756delinsGGGTGAT	GRCh38
NC_000011.9:g.67816217_67816223delinsGGGTGAT , CM000673.1:g.67816217_67816223delinsGGGTGAT	GRCh37
NC_000011.8:g.67572793_67572799delinsGGGTGAT	NCBI36
NG_007878.1:g.14735_14741delinsGGGTGAT , LRG_115:g.14735_14741delinsGGGTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.180-129_180-123delinsGGGTGAT
ENST00000698254.1:c.1084-129_1084-123delinsGGGTGAT	ENSP00000513629.1:n.1084-129_1084-123delinsGGGTGAT
ENST00000698255.1:c.1504-129_1504-123delinsGGGTGAT	ENSP00000513630.1:n.1504-129_1504-123delinsGGGTGAT
ENST00000698256.1:c.1021-129_1021-123delinsGGGTGAT
ENST00000698257.1:n.973-129_973-123delinsGGGTGAT
ENST00000698258.1:n.690-129_690-123delinsGGGTGAT
ENST00000698259.1:n.456-129_456-123delinsGGGTGAT
ENST00000265686.8:c.1555-129_1555-123delinsGGGTGAT MANE Select	ENSP00000265686.3:n.1555-129_1555-123delinsGGGTGAT
ENST00000265686.7:c.1555-129_1555-123delinsGGGTGAT	ENSP00000265686.3:n.1555-129_1555-123delinsGGGTGAT
ENST00000525724.5:n.867-129_867-123delinsGGGTGAT
ENST00000528981.5:c.707-129_707-123delinsGGGTGAT
ENST00000532635.5:c.907-129_907-123delinsGGGTGAT	ENSP00000434407.1:n.907-129_907-123delinsGGGTGAT
ENST00000533005.5:n.668-129_668-123delinsGGGTGAT
NM_006019.3:c.1555-129_1555-123delinsGGGTGAT	NP_006010.2:n.1555-129_1555-123delinsGGGTGAT
NM_006053.3:c.907-129_907-123delinsGGGTGAT	NP_006044.1:n.907-129_907-123delinsGGGTGAT
XM_005273709.2:c.1555-129_1555-123delinsGGGTGAT	XP_005273766.1:n.1555-129_1555-123delinsGGGTGAT
XM_011544726.1:c.1555-129_1555-123delinsGGGTGAT	XP_011543028.1:n.1555-129_1555-123delinsGGGTGAT
XM_011544727.1:c.1555-129_1555-123delinsGGGTGAT	XP_011543029.1:n.1555-129_1555-123delinsGGGTGAT
XM_011544728.1:c.1555-129_1555-123delinsGGGTGAT	XP_011543030.1:n.1555-129_1555-123delinsGGGTGAT
XR_949754.1:n.1559-129_1559-123delinsGGGTGAT
NM_001351059.1:c.661-129_661-123delinsGGGTGAT	NP_001337988.1:n.661-129_661-123delinsGGGTGAT
XM_024448320.1:c.1648-129_1648-123delinsGGGTGAT	XP_024304088.1:n.1648-129_1648-123delinsGGGTGAT
XM_024448321.1:c.1648-129_1648-123delinsGGGTGAT	XP_024304089.1:n.1648-129_1648-123delinsGGGTGAT
XM_024448322.1:c.1648-129_1648-123delinsGGGTGAT	XP_024304090.1:n.1648-129_1648-123delinsGGGTGAT
XM_024448323.1:c.1648-129_1648-123delinsGGGTGAT	XP_024304091.1:n.1648-129_1648-123delinsGGGTGAT
XM_024448324.1:c.1648-129_1648-123delinsGGGTGAT	XP_024304092.1:n.1648-129_1648-123delinsGGGTGAT
XR_001747721.2:n.1679-129_1679-123delinsGGGTGAT
XR_001747722.1:n.1692-129_1692-123delinsGGGTGAT
XR_001747723.2:n.1692-129_1692-123delinsGGGTGAT
XR_002957115.1:n.1770-129_1770-123delinsGGGTGAT
NM_006019.4:c.1555-129_1555-123delinsGGGTGAT MANE Select	NP_006010.2:n.1555-129_1555-123delinsGGGTGAT
NM_001351059.2:c.661-129_661-123delinsGGGTGAT	NP_001337988.1:n.661-129_661-123delinsGGGTGAT
NM_006053.4:c.907-129_907-123delinsGGGTGAT	NP_006044.1:n.907-129_907-123delinsGGGTGAT