Canonical Allele Identifier: CA2636261058

Gene: TTC19

Linked Data

• gnomAD v4: 17-16006454-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16006454T>G , CM000679.2:g.16006454T>G	GRCh38
NC_000017.10:g.15909768T>G , CM000679.1:g.15909768T>G	GRCh37
NC_000017.9:g.15850493T>G	NCBI36
NG_029806.1:g.12075T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.582-20T>G MANE Select	ENSP00000261647.5:n.582-20T>G
ENST00000261647.9:c.582-20T>G	ENSP00000261647.5:n.582-20T>G
ENST00000475723.5:c.766-20T>G
ENST00000497842.6:n.692-20T>G
NM_001271420.1:c.261-20T>G	NP_001258349.1:n.261-20T>G
NM_017775.3:c.582-20T>G	NP_060245.3:n.582-20T>G
XM_011523950.1:c.582-20T>G	XP_011522252.1:n.582-20T>G
XR_934261.1:n.1791+709A>C
XM_017024801.2:c.582-20T>G	XP_016880290.2:n.582-20T>G
XM_017024802.2:c.582-20T>G	XP_016880291.2:n.582-20T>G
XM_024450814.1:c.582-20T>G	XP_024306582.1:n.582-20T>G
NM_017775.4:c.582-20T>G MANE Select	NP_060245.3:n.582-20T>G
NM_001271420.2:c.261-20T>G	NP_001258349.1:n.261-20T>G