Canonical Allele Identifier: CA2636259607

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999783-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999784del , CM000679.2:g.15999784del	GRCh38
NC_000017.10:g.15903098del , CM000679.1:g.15903098del	GRCh37
NC_000017.9:g.15843823del	NCBI36
NG_029806.1:g.5405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-65del	ENSP00000261647.5:n.-65del
ENST00000466729.5:c.1del
NM_001271420.1:c.-523del	NP_001258349.1:n.-523del
NM_017775.3:c.-65del	NP_060245.3:n.-65del
XM_011523950.1:c.-65del	XP_011522252.1:n.-65del
XM_017024801.2:c.-65del	XP_016880290.2:n.-65del
XM_017024802.2:c.-65del	XP_016880291.2:n.-65del
XM_024450814.1:c.-65del	XP_024306582.1:n.-65del