Canonical Allele Identifier: CA1242758690
Gene: TTC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32640460A= , CM000664.2:g.32640460A= GRCh38
NC_000002.11:g.32865527A= , CM000664.1:g.32865527A= GRCh37
NC_000002.10:g.32719031A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317907.9:c.537+50A= MANE Select ENSP00000313953.4:n.537+50A=
ENST00000647819.1:c.537+50A= ENSP00000497009.1:n.537+50A=
ENST00000317907.8:c.537+50A= ENSP00000313953.4:n.537+50A=
ENST00000454690.1:c.88+12080A= ENSP00000392883.1:n.88+12080A=
NM_001193509.1:c.387+50A= NP_001180438.1:n.387+50A=
NM_017735.4:c.537+50A= NP_060205.3:n.537+50A=
XM_005264416.1:c.537+50A= XP_005264473.1:n.537+50A=
XM_011532958.1:c.537+50A= XP_011531260.1:n.537+50A=
XM_005264416.2:c.537+50A= XP_005264473.1:n.537+50A=
XM_011532958.2:c.537+50A= XP_011531260.1:n.537+50A=
XR_002959314.1:n.795+50A=
NM_017735.5:c.537+50A= MANE Select NP_060205.3:n.537+50A=
NM_001193509.2:c.387+50A= NP_001180438.1:n.387+50A=