Canonical Allele Identifier: CA1242758710

Gene: TTC27

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32640490C= , CM000664.2:g.32640490C=	GRCh38
NC_000002.11:g.32865557C= , CM000664.1:g.32865557C=	GRCh37
NC_000002.10:g.32719061C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317907.9:c.537+80C= MANE Select	ENSP00000313953.4:n.537+80C=
ENST00000647819.1:c.537+80C=	ENSP00000497009.1:n.537+80C=
ENST00000317907.8:c.537+80C=	ENSP00000313953.4:n.537+80C=
ENST00000454690.1:c.88+12110C=	ENSP00000392883.1:n.88+12110C=
NM_001193509.1:c.387+80C=	NP_001180438.1:n.387+80C=
NM_017735.4:c.537+80C=	NP_060205.3:n.537+80C=
XM_005264416.1:c.537+80C=	XP_005264473.1:n.537+80C=
XM_011532958.1:c.537+80C=	XP_011531260.1:n.537+80C=
XM_005264416.2:c.537+80C=	XP_005264473.1:n.537+80C=
XM_011532958.2:c.537+80C=	XP_011531260.1:n.537+80C=
XR_002959314.1:n.795+80C=
NM_017735.5:c.537+80C= MANE Select	NP_060205.3:n.537+80C=
NM_001193509.2:c.387+80C=	NP_001180438.1:n.387+80C=