Canonical Allele Identifier: CA398381787

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15903163A>T (hg19) ; chr17:g.15999849A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999849A>T , CM000679.2:g.15999849A>T	GRCh38
NC_000017.10:g.15903163A>T , CM000679.1:g.15903163A>T	GRCh37
NC_000017.9:g.15843888A>T	NCBI36
NG_029806.1:g.5470A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1A>T MANE Select	ENSP00000261647.5:p.Met1Leu
ENST00000261647.9:c.1A>T	ENSP00000261647.5:p.Met1Leu
ENST00000466729.5:c.66A>T
ENST00000470399.1:c.16A>T	ENSP00000465082.1:p.Met6Leu
ENST00000475723.5:c.48A>T
ENST00000497842.6:n.26A>T
ENST00000583704.1:n.26A>T
NM_001271420.1:c.-458A>T	NP_001258349.1:n.-458A>T
NM_017775.3:c.1A>T	NP_060245.3:p.Met1Leu
XM_011523950.1:c.1A>T	XP_011522252.1:p.Met1Leu
XM_017024801.2:c.1A>T	XP_016880290.2:p.Met1Leu
XM_017024802.2:c.1A>T	XP_016880291.2:p.Met1Leu
XM_024450814.1:c.1A>T	XP_024306582.1:p.Met1Leu
NM_017775.4:c.1A>T MANE Select	NP_060245.3:p.Met1Leu
NM_001271420.2:c.-458A>T	NP_001258349.1:n.-458A>T