Canonical Allele Identifier: CA537310042

Gene: TANC1

Linked Data

• dbSNP Id: rs1336574316
• gnomAD v2: 2-159851459-TCACTC-T
• MyVariant Identifiers: chr2:g.159851460_159851464del (hg19) ; chr2:g.158994948_158994952del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.158994950_158994954del , CM000664.2:g.158994950_158994954del	GRCh38
NC_000002.11:g.159851462_159851466del , CM000664.1:g.159851462_159851466del	GRCh37
NC_000002.10:g.159559708_159559712del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000263635.8:c.-125-6130_-125-6126del MANE Select	ENSP00000263635.6:n.-125-6130_-125-6126de...
ENST00000263635.7:c.-125-6130_-125-6126del	ENSP00000263635.6:n.-125-6130_-125-6126de...
ENST00000454300.5:c.-443-6130_-443-6126del	ENSP00000396339.2:n.-443-6130_-443-6126de...
NM_001145909.1:c.-125-6130_-125-6126del	NP_001139381.1:n.-125-6130_-125-6126del
NM_033394.2:c.-125-6130_-125-6126del	NP_203752.2:n.-125-6130_-125-6126del
XM_006712810.2:c.-16+26168_-16+26172del	XP_006712873.1:n.-16+26168_-16+26172del
XM_006712812.2:c.-125-6130_-125-6126del	XP_006712875.1:n.-125-6130_-125-6126del
XM_011512048.1:c.-242-6130_-242-6126del	XP_011510350.1:n.-242-6130_-242-6126del
XM_011512051.1:c.-125-6130_-125-6126del	XP_011510353.1:n.-125-6130_-125-6126del
XM_011512053.1:c.-16+26168_-16+26172del	XP_011510355.1:n.-16+26168_-16+26172del
XM_011512055.1:c.-125-6130_-125-6126del	XP_011510357.1:n.-125-6130_-125-6126del
XM_011512058.1:c.-125-6130_-125-6126del	XP_011510360.1:n.-125-6130_-125-6126del
NM_001350062.1:c.-125-6130_-125-6126del	NP_001336991.1:n.-125-6130_-125-6126del
NM_001350063.1:c.-125-6130_-125-6126del	NP_001336992.1:n.-125-6130_-125-6126del
NM_001350064.1:c.-125-6130_-125-6126del	NP_001336993.1:n.-125-6130_-125-6126del
NM_001350065.1:c.-294-6130_-294-6126del	NP_001336994.1:n.-294-6130_-294-6126del
NR_146421.1:n.150-6130_150-6126del
XM_006712810.3:c.-16+26168_-16+26172del	XP_006712873.1:n.-16+26168_-16+26172del
XM_006712812.3:c.-125-6130_-125-6126del	XP_006712875.1:n.-125-6130_-125-6126del
XM_011512048.2:c.-242-6130_-242-6126del	XP_011510350.1:n.-242-6130_-242-6126del
XM_011512051.2:c.-125-6130_-125-6126del	XP_011510353.1:n.-125-6130_-125-6126del
XM_011512053.2:c.-16+26168_-16+26172del	XP_011510355.1:n.-16+26168_-16+26172del
XM_011512055.2:c.-125-6130_-125-6126del	XP_011510357.1:n.-125-6130_-125-6126del
XM_011512058.2:c.-125-6130_-125-6126del	XP_011510360.1:n.-125-6130_-125-6126del
XM_017005142.1:c.-422-6130_-422-6126del	XP_016860631.1:n.-422-6130_-422-6126del
XM_017005145.1:c.-294-6130_-294-6126del	XP_016860634.1:n.-294-6130_-294-6126del
XM_017005146.1:c.-125-6130_-125-6126del	XP_016860635.1:n.-125-6130_-125-6126del
XM_017005154.1:c.-294-6130_-294-6126del	XP_016860643.1:n.-294-6130_-294-6126del
XR_002959352.1:n.142-6130_142-6126del
XR_002959353.1:n.142-6130_142-6126del
NM_033394.3:c.-125-6130_-125-6126del MANE Select	NP_203752.2:n.-125-6130_-125-6126del
NR_146421.2:n.144-6130_144-6126del
NM_001145909.2:c.-125-6130_-125-6126del	NP_001139381.1:n.-125-6130_-125-6126del
NM_001350062.2:c.-125-6130_-125-6126del	NP_001336991.1:n.-125-6130_-125-6126del
NM_001350063.2:c.-125-6130_-125-6126del	NP_001336992.1:n.-125-6130_-125-6126del
NM_001350064.2:c.-125-6130_-125-6126del	NP_001336993.1:n.-125-6130_-125-6126del
NM_001350065.2:c.-294-6130_-294-6126del	NP_001336994.1:n.-294-6130_-294-6126del