Canonical Allele Identifier: CA2838202841

Gene: TTC27

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32766541C>T , CM000664.2:g.32766541C>T	GRCh38
NC_000002.11:g.32991608C>T , CM000664.1:g.32991608C>T	GRCh37
NC_000002.10:g.32845112C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317907.9:c.1680+8022C>T MANE Select	ENSP00000313953.4:n.1680+8022C>T
ENST00000647819.1:c.*885+8022C>T	ENSP00000497009.1:n.*885+8022C>T
ENST00000317907.8:c.1680+8022C>T	ENSP00000313953.4:n.1680+8022C>T
ENST00000433416.5:c.334C>T
NM_001193509.1:c.1530+8022C>T	NP_001180438.1:n.1530+8022C>T
NM_017735.4:c.1680+8022C>T	NP_060205.3:n.1680+8022C>T
XM_005264416.1:c.1557+8022C>T	XP_005264473.1:n.1557+8022C>T
XM_011532958.1:c.1680+8022C>T	XP_011531260.1:n.1680+8022C>T
XM_005264416.2:c.1557+8022C>T	XP_005264473.1:n.1557+8022C>T
XM_011532958.2:c.1680+8022C>T	XP_011531260.1:n.1680+8022C>T
XR_002959314.1:n.1938+8022C>T
NM_017735.5:c.1680+8022C>T MANE Select	NP_060205.3:n.1680+8022C>T
NM_001193509.2:c.1530+8022C>T	NP_001180438.1:n.1530+8022C>T