Canonical Allele Identifier: CA390466227

Gene: TTLL5

Linked Data

• MyVariant Identifiers: chr14:g.76230962A>T (hg19) ; chr14:g.75764619A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75764619A>T , CM000676.2:g.75764619A>T	GRCh38
NC_000014.8:g.76230962A>T , CM000676.1:g.76230962A>T	GRCh37
NC_000014.7:g.75300715A>T	NCBI36
NG_016974.1:g.108412A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298832.14:c.1555A>T MANE Select	ENSP00000298832.9:p.Thr519Ser
ENST00000298832.13:c.1555A>T	ENSP00000298832.9:p.Thr519Ser
ENST00000554510.5:c.82A>T	ENSP00000451946.1:p.Thr28Ser
ENST00000555422.5:n.861A>T
ENST00000556893.5:c.208A>T	ENSP00000452524.1:p.Thr70Ser
ENST00000556976.1:n.289A>T
ENST00000557636.5:c.1597A>T	ENSP00000450713.1:p.Thr533Ser
NM_015072.4:c.1555A>T	NP_055887.3:p.Thr519Ser
NM_015072.5:c.1555A>T MANE Select	NP_055887.3:p.Thr519Ser