Canonical Allele Identifier: CA425468426

Gene: TTC27

Linked Data

• MyVariant Identifiers: chr2:g.32865423G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32640356G>A , CM000664.2:g.32640356G>A	GRCh38
NC_000002.11:g.32865423G>A , CM000664.1:g.32865423G>A	GRCh37
NC_000002.10:g.32718927G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317907.9:c.483G>A MANE Select	ENSP00000313953.4:p.Leu161=
ENST00000647819.1:c.483G>A	ENSP00000497009.1:p.Leu161=
ENST00000317907.8:c.483G>A	ENSP00000313953.4:p.Leu161=
ENST00000448773.5:c.333G>A	ENSP00000393327.1:p.Leu111=
ENST00000454690.1:c.88+11976G>A	ENSP00000392883.1:n.88+11976G>A
NM_001193509.1:c.333G>A	NP_001180438.1:p.Leu111=
NM_017735.4:c.483G>A	NP_060205.3:p.Leu161=
XM_005264416.1:c.483G>A	XP_005264473.1:p.Leu161=
XM_011532958.1:c.483G>A	XP_011531260.1:p.Leu161=
XM_005264416.2:c.483G>A	XP_005264473.1:p.Leu161=
XM_011532958.2:c.483G>A	XP_011531260.1:p.Leu161=
XR_002959314.1:n.741G>A
NM_017735.5:c.483G>A MANE Select	NP_060205.3:p.Leu161=
NM_001193509.2:c.333G>A	NP_001180438.1:p.Leu111=