Canonical Allele Identifier: CA939090233
Gene: TCIRG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68047688_68047689insTTA , CM000673.2:g.68047688_68047689insTTA GRCh38
NC_000011.9:g.67815155_67815156insTTA , CM000673.1:g.67815155_67815156insTTA GRCh37
NC_000011.8:g.67571731_67571732insTTA NCBI36
NG_007878.1:g.13673_13674insTTA , LRG_115:g.13673_13674insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698254.1:c.876_877insTTA ENSP00000513629.1:p.Leu292_Met293insLeu
ENST00000698255.1:c.1296_1297insTTA ENSP00000513630.1:p.Leu432_Met433insLeu
ENST00000698256.1:c.813_814insTTA
ENST00000698257.1:n.765_766insTTA
ENST00000698258.1:n.405_406insTTA
ENST00000698259.1:n.171_172insTTA
ENST00000265686.8:c.1347_1348insTTA MANE Select ENSP00000265686.3:p.Leu449_Met450insLeu
ENST00000265686.7:c.1347_1348insTTA ENSP00000265686.3:p.Leu449_Met450insLeu
ENST00000525516.1:n.141_142insTTA
ENST00000525724.5:n.659_660insTTA
ENST00000528981.5:c.499_500insTTA
ENST00000529364.1:c.758_759insTTA
ENST00000532635.5:c.699_700insTTA ENSP00000434407.1:p.Leu233_Met234insLeu
ENST00000533005.5:n.383_384insTTA
NM_006019.3:c.1347_1348insTTA NP_006010.2:p.Leu449_Met450insLeu
NM_006053.3:c.699_700insTTA NP_006044.1:p.Leu233_Met234insLeu
XM_005273709.2:c.1347_1348insTTA XP_005273766.1:p.Leu449_Met450insLeu
XM_011544726.1:c.1347_1348insTTA XP_011543028.1:p.Leu449_Met450insLeu
XM_011544727.1:c.1347_1348insTTA XP_011543029.1:p.Leu449_Met450insLeu
XM_011544728.1:c.1347_1348insTTA XP_011543030.1:p.Leu449_Met450insLeu
XM_011544729.1:c.1363_1364insTTA XP_011543031.1:p.Tyr455delinsPheAsn
XR_949754.1:n.1351_1352insTTA
NM_001351059.1:c.453_454insTTA NP_001337988.1:p.Leu151_Met152insLeu
XM_024448320.1:c.1363_1364insTTA XP_024304088.1:p.Tyr455delinsPheAsn
XM_024448321.1:c.1363_1364insTTA XP_024304089.1:p.Tyr455delinsPheAsn
XM_024448322.1:c.1363_1364insTTA XP_024304090.1:p.Tyr455delinsPheAsn
XM_024448323.1:c.1363_1364insTTA XP_024304091.1:p.Tyr455delinsPheAsn
XM_024448324.1:c.1363_1364insTTA XP_024304092.1:p.Tyr455delinsPheAsn
XR_001747721.2:n.1471_1472insTTA
XR_001747722.1:n.1484_1485insTTA
XR_001747723.2:n.1484_1485insTTA
XR_002957115.1:n.1485_1486insTTA
NM_006019.4:c.1347_1348insTTA MANE Select NP_006010.2:p.Leu449_Met450insLeu
NM_001351059.2:c.453_454insTTA NP_001337988.1:p.Leu151_Met152insLeu
NM_006053.4:c.699_700insTTA NP_006044.1:p.Leu233_Met234insLeu