Canonical Allele Identifier: CA2636262755

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028168-AAAATGGGGGTGTTTATATAAAACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028172_16028195del , CM000679.2:g.16028172_16028195del	GRCh38
NC_000017.10:g.15931486_15931509del , CM000679.1:g.15931486_15931509del	GRCh37
NC_000017.9:g.15872211_15872234del	NCBI36
NG_029806.1:g.33793_33816del
NG_047111.1:g.193555_193578del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*650_*673del MANE Select	ENSP00000261647.5:n.*650_*673del
ENST00000261647.9:c.*650_*673del	ENSP00000261647.5:n.*650_*673del
ENST00000465567.1:n.2187_2210del
ENST00000470649.1:c.247+1470_247+1493del	ENSP00000465627.1:n.247+1470_247+1493del
ENST00000475723.5:c.1977_2000del
ENST00000481107.1:n.2461_2484del
NM_001271420.1:c.*650_*673del	NP_001258349.1:n.*650_*673del
NM_017775.3:c.*650_*673del	NP_060245.3:n.*650_*673del
XM_017024801.2:c.994+1470_994+1493del	XP_016880290.2:n.994+1470_994+1493del
XM_017024802.2:c.994+1470_994+1493del	XP_016880291.2:n.994+1470_994+1493del
NM_017775.4:c.*650_*673del MANE Select	NP_060245.3:n.*650_*673del
NM_001271420.2:c.*650_*673del	NP_001258349.1:n.*650_*673del