Canonical Allele Identifier: CA283366645

Gene: NIP7

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69339948C>T , CM000678.2:g.69339948C>T	GRCh38
NC_000016.9:g.69373851C>T , CM000678.1:g.69373851C>T	GRCh37
NC_000016.8:g.67931352C>T	NCBI36
NG_009013.1:g.4676G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016101.5:c.57-58C>T MANE Select	NP_057185.1:n.57-58C>T
ENST00000254940.10:c.57-58C>T MANE Select	ENSP00000254940.5:n.57-58C>T
NM_001199434.1:c.57-58C>T	NP_001186363.1:n.57-58C>T
NM_001199434.2:c.57-58C>T	NP_001186363.1:n.57-58C>T
NM_016101.4:c.57-58C>T	NP_057185.1:n.57-58C>T
ENST00000254940.9:c.57-58C>T	ENSP00000254940.5:n.57-58C>T
ENST00000254941.6:c.57-58C>T	ENSP00000254941.6:n.57-58C>T
ENST00000563364.2:n.22C>T
ENST00000563364.3:n.1953C>T
ENST00000563634.1:c.3-3236G>A	ENSP00000454500.1:n.3-3236G>A
ENST00000564737.1:c.467-3236G>A
ENST00000565034.1:n.57-58C>T
ENST00000569637.6:c.57-58C>T	ENSP00000463739.1:n.57-58C>T
ENST00000570293.5:c.317-3236G>A	ENSP00000464417.1:n.317-3236G>A