Canonical Allele Identifier: CA381585110
Gene: TCIRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68048925A>G , CM000673.2:g.68048925A>G GRCh38
NC_000011.9:g.67816392A>G , CM000673.1:g.67816392A>G GRCh37
NC_000011.8:g.67572968A>G NCBI36
NG_007878.1:g.14910A>G , LRG_115:g.14910A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000530449.2:n.226A>G
ENST00000698254.1:c.1130A>G ENSP00000513629.1:p.Lys377Arg
ENST00000698255.1:c.1550A>G ENSP00000513630.1:p.Lys517Arg
ENST00000698256.1:c.1067A>G
ENST00000698257.1:n.1019A>G
ENST00000698258.1:n.736A>G
ENST00000698259.1:n.502A>G
ENST00000265686.8:c.1601A>G MANE Select ENSP00000265686.3:p.Lys534Arg
ENST00000265686.7:c.1601A>G ENSP00000265686.3:p.Lys534Arg
ENST00000525724.5:n.913A>G
ENST00000528981.5:c.753A>G
ENST00000532635.5:c.953A>G ENSP00000434407.1:p.Lys318Arg
ENST00000533005.5:n.714A>G
NM_006019.3:c.1601A>G NP_006010.2:p.Lys534Arg
NM_006053.3:c.953A>G NP_006044.1:p.Lys318Arg
XM_005273709.2:c.1601A>G XP_005273766.1:p.Lys534Arg
XM_011544726.1:c.1601A>G XP_011543028.1:p.Lys534Arg
XM_011544727.1:c.1601A>G XP_011543029.1:p.Lys534Arg
XM_011544728.1:c.1601A>G XP_011543030.1:p.Lys534Arg
XR_949754.1:n.1605A>G
NM_001351059.1:c.707A>G NP_001337988.1:p.Lys236Arg
XM_024448320.1:c.1694A>G XP_024304088.1:p.Lys565Arg
XM_024448321.1:c.1694A>G XP_024304089.1:p.Lys565Arg
XM_024448322.1:c.1694A>G XP_024304090.1:p.Lys565Arg
XM_024448323.1:c.1694A>G XP_024304091.1:p.Lys565Arg
XM_024448324.1:c.1694A>G XP_024304092.1:p.Lys565Arg
XR_001747721.2:n.1725A>G
XR_001747722.1:n.1738A>G
XR_001747723.2:n.1738A>G
XR_002957115.1:n.1816A>G
NM_006019.4:c.1601A>G MANE Select NP_006010.2:p.Lys534Arg
NM_001351059.2:c.707A>G NP_001337988.1:p.Lys236Arg
NM_006053.4:c.953A>G NP_006044.1:p.Lys318Arg