Canonical Allele Identifier: CA394295453

Gene: NTHL1

Linked Data

• ClinVar Variation Id: 1371438
• ClinVar RCV Id: RCV001878999
• dbSNP Id: rs2150945430
• MyVariant Identifiers: chr16:g.2096178A>C (hg19) ; chr16:g.2046177A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2046177A>C , CM000678.2:g.2046177A>C	GRCh38
NC_000016.9:g.2096178A>C , CM000678.1:g.2096178A>C	GRCh37
NC_000016.8:g.2036179A>C	NCBI36
NG_005895.1:g.1872A>C , LRG_487:g.1872A>C
NG_008412.1:g.6690T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651522.1:c.14T>G	ENSP00000498290.1:p.Val5Gly
ENST00000651570.2:c.305T>G MANE Select	ENSP00000498421.1:p.Val102Gly
ENST00000651583.1:c.260T>G	ENSP00000498821.1:p.Val87Gly
ENST00000219066.5:c.329T>G	ENSP00000219066.1:p.Val110Gly
ENST00000561841.1:c.225T>G
ENST00000562120.1:n.38T>G
ENST00000566380.5:c.268T>G
ENST00000568513.5:c.173+103T>G
NM_002528.5:c.329T>G	NP_002519.1:p.Val110Gly
XM_011522505.1:c.329T>G	XP_011520807.1:p.Val110Gly
NM_001318193.1:c.329T>G	NP_001305122.1:p.Val110Gly
NM_001318194.1:c.24+103T>G	NP_001305123.1:n.24+103T>G
NM_002528.6:c.329T>G	NP_002519.1:p.Val110Gly
XM_017023253.1:c.329T>G	XP_016878742.1:p.Val110Gly
NM_001318193.2:c.305T>G	NP_001305122.2:p.Val102Gly
NM_002528.7:c.305T>G MANE Select	NP_002519.2:p.Val102Gly
NM_001318194.2:c.24+103T>G	NP_001305123.1:n.24+103T>G