Canonical Allele Identifier: CA2576933831

Gene: TTC27

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32640469A>G , CM000664.2:g.32640469A>G	GRCh38
NC_000002.11:g.32865536A>G , CM000664.1:g.32865536A>G	GRCh37
NC_000002.10:g.32719040A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317907.9:c.537+59A>G MANE Select	ENSP00000313953.4:n.537+59A>G
ENST00000647819.1:c.537+59A>G	ENSP00000497009.1:n.537+59A>G
ENST00000317907.8:c.537+59A>G	ENSP00000313953.4:n.537+59A>G
ENST00000454690.1:c.88+12089A>G	ENSP00000392883.1:n.88+12089A>G
NM_001193509.1:c.387+59A>G	NP_001180438.1:n.387+59A>G
NM_017735.4:c.537+59A>G	NP_060205.3:n.537+59A>G
XM_005264416.1:c.537+59A>G	XP_005264473.1:n.537+59A>G
XM_011532958.1:c.537+59A>G	XP_011531260.1:n.537+59A>G
XM_005264416.2:c.537+59A>G	XP_005264473.1:n.537+59A>G
XM_011532958.2:c.537+59A>G	XP_011531260.1:n.537+59A>G
XR_002959314.1:n.795+59A>G
NM_017735.5:c.537+59A>G MANE Select	NP_060205.3:n.537+59A>G
NM_001193509.2:c.387+59A>G	NP_001180438.1:n.387+59A>G