Canonical Allele Identifier: CA346531569

Gene: TTC27

Linked Data

• MyVariant Identifiers: chr2:g.32865431C>G (hg19) ; chr2:g.32640364C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32640364C>G , CM000664.2:g.32640364C>G	GRCh38
NC_000002.11:g.32865431C>G , CM000664.1:g.32865431C>G	GRCh37
NC_000002.10:g.32718935C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317907.9:c.491C>G MANE Select	ENSP00000313953.4:p.Ala164Gly
ENST00000647819.1:c.491C>G	ENSP00000497009.1:p.Ala164Gly
ENST00000317907.8:c.491C>G	ENSP00000313953.4:p.Ala164Gly
ENST00000448773.5:c.341C>G	ENSP00000393327.1:p.Ala114Gly
ENST00000454690.1:c.88+11984C>G	ENSP00000392883.1:n.88+11984C>G
NM_001193509.1:c.341C>G	NP_001180438.1:p.Ala114Gly
NM_017735.4:c.491C>G	NP_060205.3:p.Ala164Gly
XM_005264416.1:c.491C>G	XP_005264473.1:p.Ala164Gly
XM_011532958.1:c.491C>G	XP_011531260.1:p.Ala164Gly
XM_005264416.2:c.491C>G	XP_005264473.1:p.Ala164Gly
XM_011532958.2:c.491C>G	XP_011531260.1:p.Ala164Gly
XR_002959314.1:n.749C>G
NM_017735.5:c.491C>G MANE Select	NP_060205.3:p.Ala164Gly
NM_001193509.2:c.341C>G	NP_001180438.1:p.Ala114Gly