Canonical Allele Identifier: CA823894557

Gene: NCR3

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31588932A>T , CM000668.2:g.31588932A>T	GRCh38
NC_000006.11:g.31556709A>T , CM000668.1:g.31556709A>T	GRCh37
NC_000006.10:g.31664688A>T	NCBI36
NG_021176.1:g.9054T>A
NG_030378.1:g.7754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340027.10:c.*135T>A MANE Select	ENSP00000342156.5:n.*135T>A
ENST00000340027.9:c.*135T>A	ENSP00000342156.5:n.*135T>A
ENST00000376073.8:c.*262T>A	ENSP00000365241.4:n.*262T>A
ENST00000491161.1:n.856T>A
ENST00000495600.5:n.548T>A
NM_001145466.1:c.*262T>A	NP_001138938.1:n.*262T>A
NM_147130.2:c.*135T>A	NP_667341.1:n.*135T>A
XM_006715049.2:c.*135T>A	XP_006715112.1:n.*135T>A
XM_011514459.1:c.*135T>A	XP_011512761.1:n.*135T>A
XM_006715049.3:c.*135T>A	XP_006715112.1:n.*135T>A
XM_011514459.2:c.*135T>A	XP_011512761.1:n.*135T>A
NM_147130.3:c.*135T>A MANE Select	NP_667341.1:n.*135T>A
NM_001145466.2:c.*262T>A	NP_001138938.1:n.*262T>A