Canonical Allele Identifier: CA304335417

Gene: NFIC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3411829G>A , CM000681.2:g.3411829G>A	GRCh38
NC_000019.9:g.3411827G>A , CM000681.1:g.3411827G>A	GRCh37
NC_000019.8:g.3362827G>A	NCBI36
NG_030333.1:g.57267G>A
NG_030333.2:g.57267G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001245002.2:c.563-13277G>A MANE Select	NP_001231931.1:n.563-13277G>A
ENST00000443272.3:c.563-13277G>A MANE Select	ENSP00000396843.2:n.563-13277G>A
NM_001245002.1:c.563-13277G>A	NP_001231931.1:n.563-13277G>A
NM_001245004.1:c.563-13277G>A	NP_001231933.1:n.563-13277G>A
NM_001245004.2:c.563-13277G>A	NP_001231933.1:n.563-13277G>A
NM_001245005.1:c.536-13277G>A	NP_001231934.1:n.536-13277G>A
NM_001245005.2:c.536-13277G>A	NP_001231934.1:n.536-13277G>A
NM_005597.3:c.563-13277G>A	NP_005588.2:n.563-13277G>A
NM_005597.4:c.563-13277G>A	NP_005588.2:n.563-13277G>A
NM_205843.2:c.536-13277G>A	NP_995315.1:n.536-13277G>A
NM_205843.3:c.536-13277G>A	NP_995315.1:n.536-13277G>A
ENST00000341919.7:c.563-13277G>A	ENSP00000342194.2:n.563-13277G>A
ENST00000395111.7:c.536-13277G>A	ENSP00000378543.2:n.536-13277G>A
ENST00000443272.2:c.563-13277G>A	ENSP00000396843.2:n.563-13277G>A
ENST00000586919.5:c.536-21689G>A	ENSP00000465177.1:n.536-21689G>A
ENST00000588839.1:n.583+651G>A
ENST00000589123.5:c.536-13277G>A	ENSP00000465655.1:n.536-13277G>A
ENST00000590282.5:c.563-13277G>A	ENSP00000466647.1:n.563-13277G>A
ENST00000641145.1:c.629-13277G>A	ENSP00000492983.1:n.629-13277G>A
XM_005259563.2:c.563-13277G>A	XP_005259620.1:n.563-13277G>A
XM_005259564.2:c.563-13277G>A	XP_005259621.1:n.563-13277G>A
XM_005259564.4:c.563-13277G>A	XP_005259621.1:n.563-13277G>A
XM_006722759.1:c.536-13277G>A	XP_006722822.1:n.536-13277G>A
XM_006722759.2:c.536-13277G>A	XP_006722822.2:n.536-13277G>A
XM_017026834.2:c.563-13277G>A	XP_016882323.1:n.563-13277G>A
XM_017026835.2:c.563-13277G>A	XP_016882324.1:n.563-13277G>A
XM_017026836.2:c.536-13277G>A	XP_016882325.1:n.536-13277G>A