Canonical Allele Identifier: CA187724278
Community Standard Title: NM_001369769.2(KIFC2):c.*616C>T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144474005C>T , CM000670.2:g.144474005C>T GRCh38
NC_000008.10:g.145699388C>T , CM000670.1:g.145699388C>T GRCh37
NC_000008.9:g.145670196C>T NCBI36
NG_030003.1:g.7331G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369769.2:c.*616C>T (KIFC2) MANE Select NP_001356698.1:n.*616C>T
NM_003923.3:c.*233G>A (FOXH1) MANE Select NP_003914.1:n.*233G>A
ENST00000377317.5:c.*233G>A (FOXH1) MANE Select ENSP00000366534.4:n.*233G>A
ENST00000645548.2:c.*616C>T (KIFC2) MANE Select ENSP00000494595.1:n.*616C>T
NM_003923.2:c.*233G>A (FOXH1) NP_003914.1:n.*233G>A
NM_145754.3:c.*555C>T (KIFC2) NP_665697.1:n.*555C>T
NM_145754.5:c.*555C>T (KIFC2) NP_665697.1:n.*555C>T
ENST00000301332.2:c.*555C>T (KIFC2) ENSP00000301332.2:n.*555C>T
ENST00000301332.3:c.*555C>T (KIFC2) ENSP00000301332.2:n.*555C>T
ENST00000377317.4:c.*233G>A (FOXH1) ENSP00000366534.4:n.*233G>A
ENST00000643461.1:n.3449C>T (KIFC2)
XM_005272357.2:c.*616C>T (KIFC2) XP_005272414.1:n.*616C>T
XM_005272357.3:c.*616C>T (KIFC2) XP_005272414.1:n.*616C>T