Canonical Allele Identifier: CA3131203
Community Standard Title: NM_012464.5(TLL1):c.2424T>C (p.Pro808=)
Gene: TLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.166078012T>C , CM000666.2:g.166078012T>C GRCh38
NC_000004.11:g.166999164T>C , CM000666.1:g.166999164T>C GRCh37
NC_000004.10:g.167218614T>C NCBI36
NG_016278.1:g.209755T>C
NG_016278.2:g.209755T>C

Transcript Alleles

HGVS Amino-acid Change
NM_012464.5:c.2424T>C MANE Select NP_036596.3:p.Pro808=
ENST00000061240.7:c.2424T>C MANE Select ENSP00000061240.2:p.Pro808=
NM_012464.4:c.2424T>C NP_036596.3:p.Pro808=
ENST00000061240.6:c.2424T>C ENSP00000061240.2:p.Pro808=
ENST00000507499.5:c.2493T>C ENSP00000426082.1:p.Pro831=
ENST00000509505.5:c.*2069T>C ENSP00000422692.1:n.*2069T>C
XM_011532212.1:c.2508T>C XP_011530514.1:p.Pro836=
XM_011532213.1:c.2361T>C XP_011530515.1:p.Pro787=
XM_011532214.1:c.1896T>C XP_011530516.1:p.Pro632=
XM_017008570.1:c.2277T>C XP_016864059.1:p.Pro759=
XM_024454194.1:c.2124T>C XP_024309962.1:p.Pro708=
XM_024454195.1:c.2124T>C XP_024309963.1:p.Pro708=