Canonical Allele Identifier: CA109785781
Community Standard Title: NM_012464.5(TLL1):c.1846+79del
Gene: TLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.166057388del , CM000666.2:g.166057388del GRCh38
NC_000004.11:g.166978540del , CM000666.1:g.166978540del GRCh37
NC_000004.10:g.167197990del NCBI36
NG_016278.1:g.189131del
NG_016278.2:g.189131del

Transcript Alleles

HGVS Amino-acid Change
NM_012464.5:c.1846+79del MANE Select NP_036596.3:n.1846+79del
ENST00000061240.7:c.1846+79del MANE Select ENSP00000061240.2:n.1846+79del
NM_012464.4:c.1846+79del NP_036596.3:n.1846+79del
ENST00000061240.6:c.1846+79del ENSP00000061240.2:n.1846+79del
ENST00000507499.5:c.1915+79del ENSP00000426082.1:n.1915+79del
ENST00000509505.5:c.*1491+79del ENSP00000422692.1:n.*1491+79del
XM_011532212.1:c.1846+79del XP_011530514.1:n.1846+79del
XM_011532213.1:c.1699+79del XP_011530515.1:n.1699+79del
XM_011532214.1:c.1318+79del XP_011530516.1:n.1318+79del
XM_017008570.1:c.1699+79del XP_016864059.1:n.1699+79del
XM_024454194.1:c.1546+79del XP_024309962.1:n.1546+79del
XM_024454195.1:c.1546+79del XP_024309963.1:n.1546+79del