Canonical Allele Identifier: CA381585002

Gene: TCIRG1

Linked Data

• MyVariant Identifiers: chr11:g.67816374G>T (hg19) ; chr11:g.68048907G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68048907G>T , CM000673.2:g.68048907G>T	GRCh38
NC_000011.9:g.67816374G>T , CM000673.1:g.67816374G>T	GRCh37
NC_000011.8:g.67572950G>T	NCBI36
NG_007878.1:g.14892G>T , LRG_115:g.14892G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530449.2:n.208G>T
ENST00000698254.1:c.1112G>T	ENSP00000513629.1:p.Ser371Ile
ENST00000698255.1:c.1532G>T	ENSP00000513630.1:p.Ser511Ile
ENST00000698256.1:c.1049G>T
ENST00000698257.1:n.1001G>T
ENST00000698258.1:n.718G>T
ENST00000698259.1:n.484G>T
ENST00000265686.8:c.1583G>T MANE Select	ENSP00000265686.3:p.Ser528Ile
ENST00000265686.7:c.1583G>T	ENSP00000265686.3:p.Ser528Ile
ENST00000525724.5:n.895G>T
ENST00000528981.5:c.735G>T
ENST00000532635.5:c.935G>T	ENSP00000434407.1:p.Ser312Ile
ENST00000533005.5:n.696G>T
NM_006019.3:c.1583G>T	NP_006010.2:p.Ser528Ile
NM_006053.3:c.935G>T	NP_006044.1:p.Ser312Ile
XM_005273709.2:c.1583G>T	XP_005273766.1:p.Ser528Ile
XM_011544726.1:c.1583G>T	XP_011543028.1:p.Ser528Ile
XM_011544727.1:c.1583G>T	XP_011543029.1:p.Ser528Ile
XM_011544728.1:c.1583G>T	XP_011543030.1:p.Ser528Ile
XR_949754.1:n.1587G>T
NM_001351059.1:c.689G>T	NP_001337988.1:p.Ser230Ile
XM_024448320.1:c.1676G>T	XP_024304088.1:p.Ser559Ile
XM_024448321.1:c.1676G>T	XP_024304089.1:p.Ser559Ile
XM_024448322.1:c.1676G>T	XP_024304090.1:p.Ser559Ile
XM_024448323.1:c.1676G>T	XP_024304091.1:p.Ser559Ile
XM_024448324.1:c.1676G>T	XP_024304092.1:p.Ser559Ile
XR_001747721.2:n.1707G>T
XR_001747722.1:n.1720G>T
XR_001747723.2:n.1720G>T
XR_002957115.1:n.1798G>T
NM_006019.4:c.1583G>T MANE Select	NP_006010.2:p.Ser528Ile
NM_001351059.2:c.689G>T	NP_001337988.1:p.Ser230Ile
NM_006053.4:c.935G>T	NP_006044.1:p.Ser312Ile