Canonical Allele Identifier: CA2749405536

Gene: TTC27

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.32640486_32640498del , CM000664.2:g.32640486_32640498del	GRCh38
NC_000002.11:g.32865553_32865565del , CM000664.1:g.32865553_32865565del	GRCh37
NC_000002.10:g.32719057_32719069del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317907.9:c.537+76_537+88del MANE Select	ENSP00000313953.4:n.537+76_537+88del
ENST00000647819.1:c.537+76_537+88del	ENSP00000497009.1:n.537+76_537+88del
ENST00000317907.8:c.537+76_537+88del	ENSP00000313953.4:n.537+76_537+88del
ENST00000454690.1:c.88+12106_88+12118del	ENSP00000392883.1:n.88+12106_88+12118del
NM_001193509.1:c.387+76_387+88del	NP_001180438.1:n.387+76_387+88del
NM_017735.4:c.537+76_537+88del	NP_060205.3:n.537+76_537+88del
XM_005264416.1:c.537+76_537+88del	XP_005264473.1:n.537+76_537+88del
XM_011532958.1:c.537+76_537+88del	XP_011531260.1:n.537+76_537+88del
XM_005264416.2:c.537+76_537+88del	XP_005264473.1:n.537+76_537+88del
XM_011532958.2:c.537+76_537+88del	XP_011531260.1:n.537+76_537+88del
XR_002959314.1:n.795+76_795+88del
NM_017735.5:c.537+76_537+88del MANE Select	NP_060205.3:n.537+76_537+88del
NM_001193509.2:c.387+76_387+88del	NP_001180438.1:n.387+76_387+88del