Canonical Allele Identifier: CA381591621

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050574C>G , CM000673.2:g.68050574C>G	GRCh38
NC_000011.9:g.67818041C>G , CM000673.1:g.67818041C>G	GRCh37
NC_000011.8:g.67574617C>G	NCBI36
NG_007878.1:g.16559C>G , LRG_115:g.16559C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.2324C>G MANE Select	NP_006010.2:p.Pro775Arg
ENST00000265686.8:c.2324C>G MANE Select	ENSP00000265686.3:p.Pro775Arg
NM_001351059.1:c.1430C>G	NP_001337988.1:p.Pro477Arg
NM_001351059.2:c.1430C>G	NP_001337988.1:p.Pro477Arg
NM_006019.3:c.2324C>G	NP_006010.2:p.Pro775Arg
NM_006053.3:c.1676C>G	NP_006044.1:p.Pro559Arg
NM_006053.4:c.1676C>G	NP_006044.1:p.Pro559Arg
ENST00000265686.7:c.2324C>G	ENSP00000265686.3:p.Pro775Arg
ENST00000525724.5:n.1636C>G
ENST00000530063.1:c.140-167C>G	ENSP00000432957.1:n.140-167C>G
ENST00000530449.1:n.452C>G
ENST00000530449.2:n.1549C>G
ENST00000530802.1:n.142+150C>G
ENST00000532635.5:c.1676C>G	ENSP00000434407.1:p.Pro559Arg
ENST00000533005.5:n.1437C>G
ENST00000698254.1:c.1853C>G	ENSP00000513629.1:p.Pro618Arg
ENST00000698255.1:c.2273C>G	ENSP00000513630.1:p.Pro758Arg
ENST00000698257.1:n.1742C>G
ENST00000698258.1:n.1459C>G
ENST00000698259.1:n.1593C>G
XM_005273709.2:c.2324C>G	XP_005273766.1:p.Pro775Arg
XM_011544726.1:c.2324C>G	XP_011543028.1:p.Pro775Arg
XM_011544727.1:c.2237-167C>G	XP_011543029.1:n.2237-167C>G
XM_024448320.1:c.2417C>G	XP_024304088.1:p.Pro806Arg
XM_024448321.1:c.2417C>G	XP_024304089.1:p.Pro806Arg
XM_024448322.1:c.2417C>G	XP_024304090.1:p.Pro806Arg
XM_024448323.1:c.2417C>G	XP_024304091.1:p.Pro806Arg
XR_001747721.2:n.2493C>G
XR_001747722.1:n.2461C>G
XR_001747723.2:n.2506C>G
XR_002957115.1:n.2682C>G
XR_949754.1:n.2471C>G