Canonical Allele Identifier: CA6146967

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68045103G>C , CM000673.2:g.68045103G>C	GRCh38
NC_000011.9:g.67812570G>C , CM000673.1:g.67812570G>C	GRCh37
NC_000011.8:g.67569146G>C	NCBI36
NG_007878.1:g.11088G>C , LRG_115:g.11088G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.1165+1G>C MANE Select	NP_006010.2:n.1165+1G>C
ENST00000265686.8:c.1165+1G>C MANE Select	ENSP00000265686.3:n.1165+1G>C
NM_001351059.1:c.271+1G>C	NP_001337988.1:n.271+1G>C
NM_001351059.2:c.271+1G>C	NP_001337988.1:n.271+1G>C
NM_006019.3:c.1165+1G>C	NP_006010.2:n.1165+1G>C
NM_006053.3:c.517+1G>C	NP_006044.1:n.517+1G>C
NM_006053.4:c.517+1G>C	NP_006044.1:n.517+1G>C
ENST00000265686.7:c.1165+1G>C	ENSP00000265686.3:n.1165+1G>C
ENST00000525724.5:n.477+1G>C
ENST00000528981.5:c.255+1G>C
ENST00000529364.1:c.576+1G>C
ENST00000532635.5:c.517+1G>C	ENSP00000434407.1:n.517+1G>C
ENST00000533005.5:n.201+1G>C
ENST00000698254.1:c.694+1G>C	ENSP00000513629.1:n.694+1G>C
ENST00000698255.1:c.1114+1G>C	ENSP00000513630.1:n.1114+1G>C
ENST00000698256.1:c.631+1G>C
ENST00000698257.1:n.583+1G>C
XM_005273709.2:c.1165+1G>C	XP_005273766.1:n.1165+1G>C
XM_011544726.1:c.1165+1G>C	XP_011543028.1:n.1165+1G>C
XM_011544727.1:c.1165+1G>C	XP_011543029.1:n.1165+1G>C
XM_011544728.1:c.1165+1G>C	XP_011543030.1:n.1165+1G>C
XM_011544729.1:c.1181+1G>C	XP_011543031.1:n.1181+1G>C
XM_024448320.1:c.1181+1G>C	XP_024304088.1:n.1181+1G>C
XM_024448321.1:c.1181+1G>C	XP_024304089.1:n.1181+1G>C
XM_024448322.1:c.1181+1G>C	XP_024304090.1:n.1181+1G>C
XM_024448323.1:c.1181+1G>C	XP_024304091.1:n.1181+1G>C
XM_024448324.1:c.1181+1G>C	XP_024304092.1:n.1181+1G>C
XR_001747721.2:n.1289+1G>C
XR_001747722.1:n.1302+1G>C
XR_001747723.2:n.1302+1G>C
XR_002957115.1:n.1303+1G>C
XR_949754.1:n.1169+1G>C