Canonical Allele Identifier: CA390465908
Community Standard Title: NM_015072.5(TTLL5):c.1487+1G>A
Gene: TTLL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75745582G>A , CM000676.2:g.75745582G>A GRCh38
NC_000014.8:g.76211925G>A , CM000676.1:g.76211925G>A GRCh37
NC_000014.7:g.75281678G>A NCBI36
NG_016974.1:g.89375G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015072.5:c.1487+1G>A MANE Select NP_055887.3:n.1487+1G>A
ENST00000298832.14:c.1487+1G>A MANE Select ENSP00000298832.9:n.1487+1G>A
NM_015072.4:c.1487+1G>A NP_055887.3:n.1487+1G>A
ENST00000298832.13:c.1487+1G>A ENSP00000298832.9:n.1487+1G>A
ENST00000554148.5:n.643+1G>A
ENST00000554510.5:c.-26+1G>A ENSP00000451946.1:n.-26+1G>A
ENST00000555422.5:n.793+1G>A
ENST00000556893.5:c.101+1G>A ENSP00000452524.1:n.101+1G>A
ENST00000556976.1:n.182+1G>A
ENST00000557636.5:c.1529+1G>A ENSP00000450713.1:n.1529+1G>A