Canonical Allele Identifier: CA350626754

Gene: NHEJ1

Linked Data

• MyVariant Identifiers: chr2:g.220011422A>C (hg19) ; chr2:g.219146700A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219146700A>C , CM000664.2:g.219146700A>C	GRCh38
NC_000002.11:g.220011422A>C , CM000664.1:g.220011422A>C	GRCh37
NC_000002.10:g.219719666A>C	NCBI36
NG_007880.1:g.19166T>G , LRG_90:g.19166T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426304.6:c.568T>G	ENSP00000394896.2:p.Leu190Val
ENST00000457600.3:c.568T>G	ENSP00000407201.2:p.Leu190Val
ENST00000698174.1:c.568T>G	ENSP00000513594.1:p.Leu190Val
ENST00000698175.1:c.*315T>G	ENSP00000513595.1:n.*315T>G
ENST00000698176.1:n.640T>G
ENST00000698202.1:c.568T>G	ENSP00000513605.1:p.Leu190Val
ENST00000698203.1:c.568T>G	ENSP00000513606.1:p.Leu190Val
ENST00000356853.10:c.568T>G MANE Select	ENSP00000349313.5:p.Leu190Val
ENST00000318673.6:c.*1690T>G	ENSP00000320919.3:n.*1690T>G
ENST00000356853.9:c.568T>G	ENSP00000349313.5:p.Leu190Val
ENST00000409720.5:c.568T>G	ENSP00000387290.1:p.Leu190Val
ENST00000418099.5:c.568T>G	ENSP00000408966.1:p.Leu190Val
ENST00000426304.5:c.328T>G	ENSP00000394896.1:p.Leu110Val
ENST00000457600.2:c.568T>G	ENSP00000407201.1:p.Leu190Val
ENST00000498327.5:n.2756T>G
NM_024782.2:c.568T>G , LRG_90t1:c.568T>G	NP_079058.1:p.Leu190Val
NM_001377498.1:c.568T>G	NP_001364427.1:p.Leu190Val
NM_001377499.1:c.568T>G	NP_001364428.1:p.Leu190Val
NM_024782.3:c.568T>G MANE Select	NP_079058.1:p.Leu190Val
NR_165304.1:n.664T>G