Canonical Allele Identifier: CA2636262748

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028162-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028162A>G , CM000679.2:g.16028162A>G	GRCh38
NC_000017.10:g.15931476A>G , CM000679.1:g.15931476A>G	GRCh37
NC_000017.9:g.15872201A>G	NCBI36
NG_029806.1:g.33783A>G
NG_047111.1:g.193585T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*640A>G MANE Select	ENSP00000261647.5:n.*640A>G
ENST00000261647.9:c.*640A>G	ENSP00000261647.5:n.*640A>G
ENST00000465567.1:n.2177A>G
ENST00000470649.1:c.247+1460A>G	ENSP00000465627.1:n.247+1460A>G
ENST00000475723.5:c.1967A>G
ENST00000481107.1:n.2451A>G
NM_001271420.1:c.*640A>G	NP_001258349.1:n.*640A>G
NM_017775.3:c.*640A>G	NP_060245.3:n.*640A>G
XM_017024801.2:c.994+1460A>G	XP_016880290.2:n.994+1460A>G
XM_017024802.2:c.994+1460A>G	XP_016880291.2:n.994+1460A>G
NM_017775.4:c.*640A>G MANE Select	NP_060245.3:n.*640A>G
NM_001271420.2:c.*640A>G	NP_001258349.1:n.*640A>G