Canonical Allele Identifier: CA398382477

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15903283C>G (hg19) ; chr17:g.15999969C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999969C>G , CM000679.2:g.15999969C>G	GRCh38
NC_000017.10:g.15903283C>G , CM000679.1:g.15903283C>G	GRCh37
NC_000017.9:g.15844008C>G	NCBI36
NG_029806.1:g.5590C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.121C>G MANE Select	ENSP00000261647.5:p.Gln41Glu
ENST00000261647.9:c.121C>G	ENSP00000261647.5:p.Gln41Glu
ENST00000466729.5:c.186C>G
ENST00000470399.1:c.136C>G	ENSP00000465082.1:p.Gln46Glu
ENST00000475723.5:c.168C>G
ENST00000497842.6:n.146C>G
ENST00000583704.1:n.146C>G
NM_001271420.1:c.-338C>G	NP_001258349.1:n.-338C>G
NM_017775.3:c.121C>G	NP_060245.3:p.Gln41Glu
XM_011523950.1:c.121C>G	XP_011522252.1:p.Gln41Glu
XM_017024801.2:c.121C>G	XP_016880290.2:p.Gln41Glu
XM_017024802.2:c.121C>G	XP_016880291.2:p.Gln41Glu
XM_024450814.1:c.121C>G	XP_024306582.1:p.Gln41Glu
NM_017775.4:c.121C>G MANE Select	NP_060245.3:p.Gln41Glu
NM_001271420.2:c.-338C>G	NP_001258349.1:n.-338C>G