Canonical Allele Identifier: CA398382584

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999993-C-G
• MyVariant Identifiers: chr17:g.15903307C>G (hg19) ; chr17:g.15999993C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999993C>G , CM000679.2:g.15999993C>G	GRCh38
NC_000017.10:g.15903307C>G , CM000679.1:g.15903307C>G	GRCh37
NC_000017.9:g.15844032C>G	NCBI36
NG_029806.1:g.5614C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.145C>G MANE Select	ENSP00000261647.5:p.Pro49Ala
ENST00000261647.9:c.145C>G	ENSP00000261647.5:p.Pro49Ala
ENST00000466729.5:c.210C>G
ENST00000470399.1:c.160C>G	ENSP00000465082.1:p.Pro54Ala
ENST00000475723.5:c.192C>G
ENST00000497842.6:n.170C>G
ENST00000583704.1:n.170C>G
NM_001271420.1:c.-314C>G	NP_001258349.1:n.-314C>G
NM_017775.3:c.145C>G	NP_060245.3:p.Pro49Ala
XM_011523950.1:c.145C>G	XP_011522252.1:p.Pro49Ala
XM_017024801.2:c.145C>G	XP_016880290.2:p.Pro49Ala
XM_017024802.2:c.145C>G	XP_016880291.2:p.Pro49Ala
XM_024450814.1:c.145C>G	XP_024306582.1:p.Pro49Ala
NM_017775.4:c.145C>G MANE Select	NP_060245.3:p.Pro49Ala
NM_001271420.2:c.-314C>G	NP_001258349.1:n.-314C>G