Canonical Allele Identifier: CA398382742

Gene: TTC19

Linked Data

• gnomAD v4: 17-16000029-G-T
• MyVariant Identifiers: chr17:g.15903343G>T (hg19) ; chr17:g.16000029G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000029G>T , CM000679.2:g.16000029G>T	GRCh38
NC_000017.10:g.15903343G>T , CM000679.1:g.15903343G>T	GRCh37
NC_000017.9:g.15844068G>T	NCBI36
NG_029806.1:g.5650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.181G>T MANE Select	ENSP00000261647.5:p.Ala61Ser
ENST00000261647.9:c.181G>T	ENSP00000261647.5:p.Ala61Ser
ENST00000466729.5:c.246G>T
ENST00000470399.1:c.196G>T	ENSP00000465082.1:p.Ala66Ser
ENST00000475723.5:c.228G>T
ENST00000497842.6:n.206G>T
ENST00000583704.1:n.206G>T
NM_001271420.1:c.-278G>T	NP_001258349.1:n.-278G>T
NM_017775.3:c.181G>T	NP_060245.3:p.Ala61Ser
XM_011523950.1:c.181G>T	XP_011522252.1:p.Ala61Ser
XM_017024801.2:c.181G>T	XP_016880290.2:p.Ala61Ser
XM_017024802.2:c.181G>T	XP_016880291.2:p.Ala61Ser
XM_024450814.1:c.181G>T	XP_024306582.1:p.Ala61Ser
NM_017775.4:c.181G>T MANE Select	NP_060245.3:p.Ala61Ser
NM_001271420.2:c.-278G>T	NP_001258349.1:n.-278G>T