Canonical Allele Identifier: CA3714675

Gene: NCR3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31590114A>C , CM000668.2:g.31590114A>C	GRCh38
NC_000006.11:g.31557891A>C , CM000668.1:g.31557891A>C	GRCh37
NC_000006.10:g.31665870A>C	NCBI36
NG_021176.1:g.7872T>G
NG_030378.1:g.8936A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340027.10:c.56T>G MANE Select	ENSP00000342156.5:p.Leu19Arg
ENST00000340027.9:c.56T>G	ENSP00000342156.5:p.Leu19Arg
ENST00000376071.4:c.56T>G	ENSP00000365239.4:p.Leu19Arg
ENST00000376072.7:c.56T>G	ENSP00000365240.3:p.Leu19Arg
ENST00000376073.8:c.56T>G	ENSP00000365241.4:p.Leu19Arg
ENST00000491161.1:n.116T>G
ENST00000495600.5:n.23-215T>G
NM_001145466.1:c.56T>G	NP_001138938.1:p.Leu19Arg
NM_001145467.1:c.56T>G	NP_001138939.1:p.Leu19Arg
NM_147130.2:c.56T>G	NP_667341.1:p.Leu19Arg
XM_006715049.2:c.56T>G	XP_006715112.1:p.Leu19Arg
XM_011514459.1:c.56T>G	XP_011512761.1:p.Leu19Arg
XM_006715049.3:c.56T>G	XP_006715112.1:p.Leu19Arg
XM_011514459.2:c.56T>G	XP_011512761.1:p.Leu19Arg
NM_147130.3:c.56T>G MANE Select	NP_667341.1:p.Leu19Arg
NM_001145466.2:c.56T>G	NP_001138938.1:p.Leu19Arg
NM_001145467.2:c.56T>G	NP_001138939.1:p.Leu19Arg