Canonical Allele Identifier: CA2249869846

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027482_16027487delinsCAAAGA , CM000679.2:g.16027482_16027487delinsCAAAGA	GRCh38
NC_000017.10:g.15930796_15930801delinsCAAAGA , CM000679.1:g.15930796_15930801delinsCAAAGA	GRCh37
NC_000017.9:g.15871521_15871526delinsCAAAGA	NCBI36
NG_029806.1:g.33103_33108delinsCAAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1103_1108delinsCAAAGA MANE Select	ENSP00000261647.5:p.Ser368=
ENST00000261647.9:c.1103_1108delinsCAAAGA	ENSP00000261647.5:p.Ser368=
ENST00000465567.1:n.1497_1502delinsCAAAGA
ENST00000470649.1:c.247+780_247+785delinsCAAAGA	ENSP00000465627.1:n.247+780_247+785delinsCAAAGA
ENST00000475723.5:c.1287_1292delinsCAAAGA
ENST00000481107.1:n.1771_1776delinsCAAAGA
ENST00000497842.6:n.1307_1312delinsCAAAGA
NM_001271420.1:c.782_787delinsCAAAGA	NP_001258349.1:p.Ser261=
NM_017775.3:c.1103_1108delinsCAAAGA	NP_060245.3:p.Ser368=
XM_017024801.2:c.994+780_994+785delinsCAAAGA	XP_016880290.2:n.994+780_994+785delinsCAAAGA
XM_017024802.2:c.994+780_994+785delinsCAAAGA	XP_016880291.2:n.994+780_994+785delinsCAAAGA
NM_017775.4:c.1103_1108delinsCAAAGA MANE Select	NP_060245.3:p.Ser368=
NM_001271420.2:c.782_787delinsCAAAGA	NP_001258349.1:p.Ser261=