Canonical Allele Identifier: CA398379617

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930829A>T (hg19) ; chr17:g.16027515A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027515A>T , CM000679.2:g.16027515A>T	GRCh38
NC_000017.10:g.15930829A>T , CM000679.1:g.15930829A>T	GRCh37
NC_000017.9:g.15871554A>T	NCBI36
NG_029806.1:g.33136A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1136A>T MANE Select	ENSP00000261647.5:p.Lys379Met
ENST00000261647.9:c.1136A>T	ENSP00000261647.5:p.Lys379Met
ENST00000465567.1:n.1530A>T
ENST00000470649.1:c.247+813A>T	ENSP00000465627.1:n.247+813A>T
ENST00000475723.5:c.1320A>T
ENST00000481107.1:n.1804A>T
ENST00000497842.6:n.1340A>T
NM_001271420.1:c.815A>T	NP_001258349.1:p.Lys272Met
NM_017775.3:c.1136A>T	NP_060245.3:p.Lys379Met
XM_017024801.2:c.994+813A>T	XP_016880290.2:n.994+813A>T
XM_017024802.2:c.994+813A>T	XP_016880291.2:n.994+813A>T
NM_017775.4:c.1136A>T MANE Select	NP_060245.3:p.Lys379Met
NM_001271420.2:c.815A>T	NP_001258349.1:p.Lys272Met