Canonical Allele Identifier: CA1242758686
Gene: TTC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32640454G= , CM000664.2:g.32640454G= GRCh38
NC_000002.11:g.32865521G= , CM000664.1:g.32865521G= GRCh37
NC_000002.10:g.32719025G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317907.9:c.537+44G= MANE Select ENSP00000313953.4:n.537+44G=
ENST00000647819.1:c.537+44G= ENSP00000497009.1:n.537+44G=
ENST00000317907.8:c.537+44G= ENSP00000313953.4:n.537+44G=
ENST00000454690.1:c.88+12074G= ENSP00000392883.1:n.88+12074G=
NM_001193509.1:c.387+44G= NP_001180438.1:n.387+44G=
NM_017735.4:c.537+44G= NP_060205.3:n.537+44G=
XM_005264416.1:c.537+44G= XP_005264473.1:n.537+44G=
XM_011532958.1:c.537+44G= XP_011531260.1:n.537+44G=
XM_005264416.2:c.537+44G= XP_005264473.1:n.537+44G=
XM_011532958.2:c.537+44G= XP_011531260.1:n.537+44G=
XR_002959314.1:n.795+44G=
NM_017735.5:c.537+44G= MANE Select NP_060205.3:n.537+44G=
NM_001193509.2:c.387+44G= NP_001180438.1:n.387+44G=