Canonical Allele Identifier: CA1242758701
Gene: TTC27 HGNC NCBI

Linked Data

dbSNP Id: rs1664601509
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32640477G>A , CM000664.2:g.32640477G>A GRCh38
NC_000002.11:g.32865544G>A , CM000664.1:g.32865544G>A GRCh37
NC_000002.10:g.32719048G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000317907.9:c.537+67G>A MANE Select ENSP00000313953.4:n.537+67G>A
ENST00000647819.1:c.537+67G>A ENSP00000497009.1:n.537+67G>A
ENST00000317907.8:c.537+67G>A ENSP00000313953.4:n.537+67G>A
ENST00000454690.1:c.88+12097G>A ENSP00000392883.1:n.88+12097G>A
NM_001193509.1:c.387+67G>A NP_001180438.1:n.387+67G>A
NM_017735.4:c.537+67G>A NP_060205.3:n.537+67G>A
XM_005264416.1:c.537+67G>A XP_005264473.1:n.537+67G>A
XM_011532958.1:c.537+67G>A XP_011531260.1:n.537+67G>A
XM_005264416.2:c.537+67G>A XP_005264473.1:n.537+67G>A
XM_011532958.2:c.537+67G>A XP_011531260.1:n.537+67G>A
XR_002959314.1:n.795+67G>A
NM_017735.5:c.537+67G>A MANE Select NP_060205.3:n.537+67G>A
NM_001193509.2:c.387+67G>A NP_001180438.1:n.387+67G>A
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