Canonical Allele Identifier: CA2576933830
Gene: TTC27 HGNC NCBI

Linked Data

gnomAD v4: 2-32640467-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32640467C>G , CM000664.2:g.32640467C>G GRCh38
NC_000002.11:g.32865534C>G , CM000664.1:g.32865534C>G GRCh37
NC_000002.10:g.32719038C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317907.9:c.537+57C>G MANE Select ENSP00000313953.4:n.537+57C>G
ENST00000647819.1:c.537+57C>G ENSP00000497009.1:n.537+57C>G
ENST00000317907.8:c.537+57C>G ENSP00000313953.4:n.537+57C>G
ENST00000454690.1:c.88+12087C>G ENSP00000392883.1:n.88+12087C>G
NM_001193509.1:c.387+57C>G NP_001180438.1:n.387+57C>G
NM_017735.4:c.537+57C>G NP_060205.3:n.537+57C>G
XM_005264416.1:c.537+57C>G XP_005264473.1:n.537+57C>G
XM_011532958.1:c.537+57C>G XP_011531260.1:n.537+57C>G
XM_005264416.2:c.537+57C>G XP_005264473.1:n.537+57C>G
XM_011532958.2:c.537+57C>G XP_011531260.1:n.537+57C>G
XR_002959314.1:n.795+57C>G
NM_017735.5:c.537+57C>G MANE Select NP_060205.3:n.537+57C>G
NM_001193509.2:c.387+57C>G NP_001180438.1:n.387+57C>G