Canonical Allele Identifier: CA624957557

Gene: TTC19

Linked Data

• dbSNP Id: rs1402193695
• gnomAD v2: 17-15931426-G-A
• gnomAD v4: 17-16028112-G-A
• MyVariant Identifiers: chr17:g.15931426G>A (hg19) ; chr17:g.16028112G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028112G>A , CM000679.2:g.16028112G>A	GRCh38
NC_000017.10:g.15931426G>A , CM000679.1:g.15931426G>A	GRCh37
NC_000017.9:g.15872151G>A	NCBI36
NG_029806.1:g.33733G>A
NG_047111.1:g.193635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*590G>A MANE Select	ENSP00000261647.5:n.*590G>A
ENST00000261647.9:c.*590G>A	ENSP00000261647.5:n.*590G>A
ENST00000465567.1:n.2127G>A
ENST00000470649.1:c.247+1410G>A	ENSP00000465627.1:n.247+1410G>A
ENST00000475723.5:c.1917G>A
ENST00000481107.1:n.2401G>A
NM_001271420.1:c.*590G>A	NP_001258349.1:n.*590G>A
NM_017775.3:c.*590G>A	NP_060245.3:n.*590G>A
XM_017024801.2:c.994+1410G>A	XP_016880290.2:n.994+1410G>A
XM_017024802.2:c.994+1410G>A	XP_016880291.2:n.994+1410G>A
NM_017775.4:c.*590G>A MANE Select	NP_060245.3:n.*590G>A
NM_001271420.2:c.*590G>A	NP_001258349.1:n.*590G>A