Canonical Allele Identifier: CA6147523

Gene: TCIRG1

Linked Data

• ClinVar Variation Id: 305822
• ClinVar RCV Id: RCV000374795 ; RCV000900453
• dbSNP Id: rs200879286
• ExAC: 11:67818138 G / A
• gnomAD v2: 11-67818138-G-A
• gnomAD v3: 11-68050671-G-A
• gnomAD v4: 11-68050671-G-A
• MyVariant Identifiers: chr11:g.67818138G>A (hg19) ; chr11:g.68050671G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68050671G>A , CM000673.2:g.68050671G>A	GRCh38
NC_000011.9:g.67818138G>A , CM000673.1:g.67818138G>A	GRCh37
NC_000011.8:g.67574714G>A	NCBI36
NG_007878.1:g.16656G>A , LRG_115:g.16656G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698254.1:c.1943+7G>A	ENSP00000513629.1:n.1943+7G>A
ENST00000698255.1:c.2363+7G>A	ENSP00000513630.1:n.2363+7G>A
ENST00000698257.1:n.1832+7G>A
ENST00000698258.1:n.1549+7G>A
ENST00000265686.8:c.2414+7G>A MANE Select	ENSP00000265686.3:n.2414+7G>A
ENST00000265686.7:c.2414+7G>A	ENSP00000265686.3:n.2414+7G>A
ENST00000525724.5:n.1726+7G>A
ENST00000530063.1:c.140-70G>A	ENSP00000432957.1:n.140-70G>A
ENST00000530802.1:n.143-70G>A
ENST00000532635.5:c.1766+7G>A	ENSP00000434407.1:n.1766+7G>A
ENST00000533005.5:n.1527+7G>A
NM_006019.3:c.2414+7G>A	NP_006010.2:n.2414+7G>A
NM_006053.3:c.1766+7G>A	NP_006044.1:n.1766+7G>A
XM_005273709.2:c.2414+7G>A	XP_005273766.1:n.2414+7G>A
XM_011544726.1:c.2414+7G>A	XP_011543028.1:n.2414+7G>A
XM_011544727.1:c.2237-70G>A	XP_011543029.1:n.2237-70G>A
XR_949754.1:n.2561+7G>A
NM_001351059.1:c.1520+7G>A	NP_001337988.1:n.1520+7G>A
XM_024448320.1:c.2507+7G>A	XP_024304088.1:n.2507+7G>A
XM_024448321.1:c.2507+7G>A	XP_024304089.1:n.2507+7G>A
XM_024448322.1:c.2507+7G>A	XP_024304090.1:n.2507+7G>A
XM_024448323.1:c.*3G>A	XP_024304091.1:n.*3G>A
XR_001747721.2:n.2583+7G>A
XR_001747722.1:n.2551+7G>A
XR_001747723.2:n.2596+7G>A
XR_002957115.1:n.2772+7G>A
NM_006019.4:c.2414+7G>A MANE Select	NP_006010.2:n.2414+7G>A
NM_001351059.2:c.1520+7G>A	NP_001337988.1:n.1520+7G>A
NM_006053.4:c.1766+7G>A	NP_006044.1:n.1766+7G>A