Canonical Allele Identifier: CA1164520096

Gene: NFYC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40757742G>C , CM000663.2:g.40757742G>C	GRCh38
NC_000001.10:g.41223414G>C , CM000663.1:g.41223414G>C	GRCh37
NC_000001.9:g.40996001G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014223.5:c.388-379G>C MANE Select	NP_055038.2:n.388-379G>C
ENST00000447388.8:c.388-379G>C MANE Select	ENSP00000404427.3:n.388-379G>C
NM_001142587.1:c.388-379G>C	NP_001136059.1:n.388-379G>C
NM_001142587.2:c.388-379G>C	NP_001136059.1:n.388-379G>C
NM_001142588.1:c.388-379G>C	NP_001136060.1:n.388-379G>C
NM_001142588.2:c.388-379G>C	NP_001136060.1:n.388-379G>C
NM_001142589.1:c.274-379G>C	NP_001136061.1:n.274-379G>C
NM_001142589.2:c.274-379G>C	NP_001136061.1:n.274-379G>C
NM_001142590.1:c.388-379G>C	NP_001136062.1:n.388-379G>C
NM_001142590.2:c.388-379G>C	NP_001136062.1:n.388-379G>C
NM_001308114.1:c.388-379G>C	NP_001295043.1:n.388-379G>C
NM_001308115.1:c.388-379G>C	NP_001295044.1:n.388-379G>C
NM_001308115.2:c.388-379G>C	NP_001295044.1:n.388-379G>C
NM_014223.4:c.388-379G>C	NP_055038.2:n.388-379G>C
ENST00000308733.9:c.388-379G>C	ENSP00000312617.5:n.388-379G>C
ENST00000372651.5:c.388-379G>C	ENSP00000361734.1:n.388-379G>C
ENST00000372652.5:c.388-379G>C	ENSP00000361736.1:n.388-379G>C
ENST00000372653.5:c.388-379G>C	ENSP00000361737.1:n.388-379G>C
ENST00000372654.5:c.388-379G>C	ENSP00000361738.1:n.388-379G>C
ENST00000372669.8:c.388-379G>C	ENSP00000361754.4:n.388-379G>C
ENST00000414185.1:c.35-379G>C
ENST00000416859.6:c.292-379G>C	ENSP00000409219.2:n.292-379G>C
ENST00000424419.6:n.296-379G>C
ENST00000425457.6:c.388-379G>C	ENSP00000396620.2:n.388-379G>C
ENST00000427410.6:c.274-379G>C	ENSP00000408315.2:n.274-379G>C
ENST00000440226.7:c.388-379G>C	ENSP00000414299.2:n.388-379G>C
ENST00000447388.7:c.388-379G>C	ENSP00000404427.3:n.388-379G>C
ENST00000456393.6:c.388-379G>C	ENSP00000408867.2:n.388-379G>C
ENST00000467203.5:n.616-379G>C
ENST00000525290.5:c.388-382G>C	ENSP00000436710.1:n.388-382G>C
ENST00000620728.4:c.82-379G>C	ENSP00000480994.1:n.82-379G>C
XM_005270894.1:c.388-379G>C	XP_005270951.1:n.388-379G>C
XM_005270895.3:c.388-379G>C	XP_005270952.3:n.388-379G>C
XM_005270895.4:c.646-379G>C	XP_005270952.4:n.646-379G>C
XM_006710658.2:c.388-379G>C	XP_006710721.2:n.388-379G>C
XM_006710658.3:c.388-379G>C	XP_006710721.2:n.388-379G>C
XM_006710660.2:c.388-379G>C	XP_006710723.2:n.388-379G>C
XM_006710660.3:c.388-379G>C	XP_006710723.2:n.388-379G>C
XM_006710661.1:c.388-379G>C	XP_006710724.1:n.388-379G>C
XM_006710661.2:c.388-379G>C	XP_006710724.1:n.388-379G>C
XM_006710662.2:c.388-379G>C	XP_006710725.2:n.388-379G>C
XM_006710662.3:c.646-379G>C	XP_006710725.3:n.646-379G>C
XM_011541516.1:c.388-379G>C	XP_011539818.1:n.388-379G>C
XM_011541517.1:c.388-379G>C	XP_011539819.1:n.388-379G>C
XM_011541517.2:c.388-379G>C	XP_011539819.1:n.388-379G>C
XM_017001364.2:c.448-379G>C	XP_016856853.1:n.448-379G>C
XM_017001365.2:c.388-379G>C	XP_016856854.1:n.388-379G>C
XM_017001366.2:c.448-379G>C	XP_016856855.1:n.448-379G>C
XM_017001367.1:c.388-379G>C	XP_016856856.1:n.388-379G>C
XM_017001368.1:c.388-379G>C	XP_016856857.1:n.388-379G>C
XM_017001369.1:c.388-379G>C	XP_016856858.1:n.388-379G>C
XM_024447354.1:c.388-379G>C	XP_024303122.1:n.388-379G>C
XM_024447355.1:c.388-379G>C	XP_024303123.1:n.388-379G>C
XM_024447356.1:c.598-379G>C	XP_024303124.1:n.598-379G>C
XM_024447357.1:c.388-379G>C	XP_024303125.1:n.388-379G>C