Canonical Allele Identifier: CA3026925065

Gene: NFIC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3466141A>T , CM000681.2:g.3466141A>T	GRCh38
NC_000019.9:g.3466139A>T , CM000681.1:g.3466139A>T	GRCh37
NC_000019.8:g.3417139A>T	NCBI36
NG_030333.1:g.111579A>T
NG_030333.2:g.111579A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001245002.2:c.*3372A>T MANE Select	NP_001231931.1:n.*3372A>T
ENST00000443272.3:c.*3372A>T MANE Select	ENSP00000396843.2:n.*3372A>T
NM_001245002.1:c.*3372A>T	NP_001231931.1:n.*3372A>T
NM_001245004.1:c.*3425A>T	NP_001231933.1:n.*3425A>T
NM_001245004.2:c.*3425A>T	NP_001231933.1:n.*3425A>T
NM_001245005.1:c.*3425A>T	NP_001231934.1:n.*3425A>T
NM_001245005.2:c.*3425A>T	NP_001231934.1:n.*3425A>T
NM_005597.3:c.*3372A>T	NP_005588.2:n.*3372A>T
NM_005597.4:c.*3372A>T	NP_005588.2:n.*3372A>T
NM_205843.2:c.*3372A>T	NP_995315.1:n.*3372A>T
NM_205843.3:c.*3372A>T	NP_995315.1:n.*3372A>T
ENST00000589123.5:c.*3372A>T	ENSP00000465655.1:n.*3372A>T
ENST00000641145.1:c.*3372A>T	ENSP00000492983.1:n.*3372A>T
XM_005259564.4:c.*3277A>T	XP_005259621.1:n.*3277A>T
XM_017026836.2:c.*3372A>T	XP_016882325.1:n.*3372A>T