Canonical Allele Identifier: CA2636259696

Gene: TTC19

Linked Data

• gnomAD v4: 17-16000019-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000020_16000021del , CM000679.2:g.16000020_16000021del	GRCh38
NC_000017.10:g.15903334_15903335del , CM000679.1:g.15903334_15903335del	GRCh37
NC_000017.9:g.15844059_15844060del	NCBI36
NG_029806.1:g.5641_5642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.172_173del MANE Select	ENSP00000261647.5:p.Pro58AlafsTer?
ENST00000261647.9:c.172_173del	ENSP00000261647.5:p.Pro58AlafsTer?
ENST00000466729.5:c.237_238del
ENST00000470399.1:c.187_188del	ENSP00000465082.1:p.Pro63AlafsTer?
ENST00000475723.5:c.219_220del
ENST00000497842.6:n.197_198del
ENST00000583704.1:n.197_198del
NM_001271420.1:c.-287_-286del	NP_001258349.1:n.-287_-286del
NM_017775.3:c.172_173del	NP_060245.3:p.Pro58AlafsTer?
XM_011523950.1:c.172_173del	XP_011522252.1:p.Pro58AlafsTer?
XM_017024801.2:c.172_173del	XP_016880290.2:p.Pro58AlafsTer?
XM_017024802.2:c.172_173del	XP_016880291.2:p.Pro58AlafsTer?
XM_024450814.1:c.172_173del	XP_024306582.1:p.Pro58AlafsTer?
NM_017775.4:c.172_173del MANE Select	NP_060245.3:p.Pro58AlafsTer?
NM_001271420.2:c.-287_-286del	NP_001258349.1:n.-287_-286del