Canonical Allele Identifier: CA2614701731

Gene: TCIRG1

Linked Data

• gnomAD v4: 11-68048874-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048874C>T , CM000673.2:g.68048874C>T	GRCh38
NC_000011.9:g.67816341C>T , CM000673.1:g.67816341C>T	GRCh37
NC_000011.8:g.67572917C>T	NCBI36
NG_007878.1:g.14859C>T , LRG_115:g.14859C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.180-5C>T
ENST00000698254.1:c.1084-5C>T	ENSP00000513629.1:n.1084-5C>T
ENST00000698255.1:c.1504-5C>T	ENSP00000513630.1:n.1504-5C>T
ENST00000698256.1:c.1021-5C>T
ENST00000698257.1:n.973-5C>T
ENST00000698258.1:n.690-5C>T
ENST00000698259.1:n.456-5C>T
ENST00000265686.8:c.1555-5C>T MANE Select	ENSP00000265686.3:n.1555-5C>T
ENST00000265686.7:c.1555-5C>T	ENSP00000265686.3:n.1555-5C>T
ENST00000525724.5:n.867-5C>T
ENST00000528981.5:c.707-5C>T
ENST00000532635.5:c.907-5C>T	ENSP00000434407.1:n.907-5C>T
ENST00000533005.5:n.668-5C>T
NM_006019.3:c.1555-5C>T	NP_006010.2:n.1555-5C>T
NM_006053.3:c.907-5C>T	NP_006044.1:n.907-5C>T
XM_005273709.2:c.1555-5C>T	XP_005273766.1:n.1555-5C>T
XM_011544726.1:c.1555-5C>T	XP_011543028.1:n.1555-5C>T
XM_011544727.1:c.1555-5C>T	XP_011543029.1:n.1555-5C>T
XM_011544728.1:c.1555-5C>T	XP_011543030.1:n.1555-5C>T
XR_949754.1:n.1559-5C>T
NM_001351059.1:c.661-5C>T	NP_001337988.1:n.661-5C>T
XM_024448320.1:c.1648-5C>T	XP_024304088.1:n.1648-5C>T
XM_024448321.1:c.1648-5C>T	XP_024304089.1:n.1648-5C>T
XM_024448322.1:c.1648-5C>T	XP_024304090.1:n.1648-5C>T
XM_024448323.1:c.1648-5C>T	XP_024304091.1:n.1648-5C>T
XM_024448324.1:c.1648-5C>T	XP_024304092.1:n.1648-5C>T
XR_001747721.2:n.1679-5C>T
XR_001747722.1:n.1692-5C>T
XR_001747723.2:n.1692-5C>T
XR_002957115.1:n.1770-5C>T
NM_006019.4:c.1555-5C>T MANE Select	NP_006010.2:n.1555-5C>T
NM_001351059.2:c.661-5C>T	NP_001337988.1:n.661-5C>T
NM_006053.4:c.907-5C>T	NP_006044.1:n.907-5C>T