Canonical Allele Identifier: CA6146778

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68043647C>T , CM000673.2:g.68043647C>T	GRCh38
NC_000011.9:g.67811114C>T , CM000673.1:g.67811114C>T	GRCh37
NC_000011.8:g.67567690C>T	NCBI36
NG_007878.1:g.9632C>T , LRG_115:g.9632C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.707C>T MANE Select	NP_006010.2:p.Thr236Met
ENST00000265686.8:c.707C>T MANE Select	ENSP00000265686.3:p.Thr236Met
NM_001351059.1:c.-204C>T	NP_001337988.1:n.-204C>T
NM_001351059.2:c.-204C>T	NP_001337988.1:n.-204C>T
NM_006019.3:c.707C>T	NP_006010.2:p.Thr236Met
NM_006053.3:c.59C>T	NP_006044.1:p.Thr20Met
NM_006053.4:c.59C>T	NP_006044.1:p.Thr20Met
ENST00000265686.7:c.707C>T	ENSP00000265686.3:p.Thr236Met
ENST00000524598.5:c.665C>T	ENSP00000432846.1:p.Thr222Met
ENST00000527530.1:n.325C>T
ENST00000529364.1:c.207C>T
ENST00000532635.5:c.59C>T	ENSP00000434407.1:p.Thr20Met
ENST00000534673.5:c.*55C>T	ENSP00000431174.1:n.*55C>T
ENST00000698254.1:c.404-552C>T	ENSP00000513629.1:n.404-552C>T
ENST00000698255.1:c.656C>T	ENSP00000513630.1:p.Thr219Met
ENST00000698256.1:c.157C>T
ENST00000698257.1:n.125C>T
XM_005273709.2:c.707C>T	XP_005273766.1:p.Thr236Met
XM_011544726.1:c.707C>T	XP_011543028.1:p.Thr236Met
XM_011544727.1:c.707C>T	XP_011543029.1:p.Thr236Met
XM_011544728.1:c.707C>T	XP_011543030.1:p.Thr236Met
XM_011544729.1:c.707C>T	XP_011543031.1:p.Thr236Met
XM_024448320.1:c.707C>T	XP_024304088.1:p.Thr236Met
XM_024448321.1:c.707C>T	XP_024304089.1:p.Thr236Met
XM_024448322.1:c.707C>T	XP_024304090.1:p.Thr236Met
XM_024448323.1:c.707C>T	XP_024304091.1:p.Thr236Met
XM_024448324.1:c.707C>T	XP_024304092.1:p.Thr236Met
XR_001747721.2:n.831C>T
XR_001747722.1:n.828C>T
XR_001747723.2:n.828C>T
XR_002957115.1:n.829C>T
XR_949754.1:n.711C>T