Canonical Allele Identifier: CA1139660824

Gene: KIFC2 FOXH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144473916G>T , CM000670.2:g.144473916G>T	GRCh38
NC_000008.10:g.145699299G>T , CM000670.1:g.145699299G>T	GRCh37
NC_000008.9:g.145670107G>T	NCBI36
NG_030003.1:g.7420C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369769.2:c.*527G>T (KIFC2) MANE Select	NP_001356698.1:n.*527G>T
NM_003923.3:c.*322C>A (FOXH1) MANE Select	NP_003914.1:n.*322C>A
ENST00000377317.5:c.*322C>A (FOXH1) MANE Select	ENSP00000366534.4:n.*322C>A
ENST00000645548.2:c.*527G>T (KIFC2) MANE Select	ENSP00000494595.1:n.*527G>T
NM_003923.2:c.*322C>A (FOXH1)	NP_003914.1:n.*322C>A
NM_145754.3:c.*466G>T (KIFC2)	NP_665697.1:n.*466G>T
NM_145754.5:c.*466G>T (KIFC2)	NP_665697.1:n.*466G>T
ENST00000301332.2:c.*466G>T (KIFC2)	ENSP00000301332.2:n.*466G>T
ENST00000301332.3:c.*466G>T (KIFC2)	ENSP00000301332.2:n.*466G>T
ENST00000377317.4:c.*322C>A (FOXH1)	ENSP00000366534.4:n.*322C>A
ENST00000643461.1:n.3360G>T (KIFC2)
XM_005272357.2:c.*527G>T (KIFC2)	XP_005272414.1:n.*527G>T
XM_005272357.3:c.*527G>T (KIFC2)	XP_005272414.1:n.*527G>T