Canonical Allele Identifier: CA398379377

Gene: TTC19

Linked Data

• dbSNP Id: rs1482892651
• MyVariant Identifiers: chr17:g.15930801A>C (hg19) ; chr17:g.16027487A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027487A>C , CM000679.2:g.16027487A>C	GRCh38
NC_000017.10:g.15930801A>C , CM000679.1:g.15930801A>C	GRCh37
NC_000017.9:g.15871526A>C	NCBI36
NG_029806.1:g.33108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1108A>C MANE Select	ENSP00000261647.5:p.Lys370Gln
ENST00000261647.9:c.1108A>C	ENSP00000261647.5:p.Lys370Gln
ENST00000465567.1:n.1502A>C
ENST00000470649.1:c.247+785A>C	ENSP00000465627.1:n.247+785A>C
ENST00000475723.5:c.1292A>C
ENST00000481107.1:n.1776A>C
ENST00000497842.6:n.1312A>C
NM_001271420.1:c.787A>C	NP_001258349.1:p.Lys263Gln
NM_017775.3:c.1108A>C	NP_060245.3:p.Lys370Gln
XM_017024801.2:c.994+785A>C	XP_016880290.2:n.994+785A>C
XM_017024802.2:c.994+785A>C	XP_016880291.2:n.994+785A>C
NM_017775.4:c.1108A>C MANE Select	NP_060245.3:p.Lys370Gln
NM_001271420.2:c.787A>C	NP_001258349.1:p.Lys263Gln