Canonical Allele Identifier: CA12268268
Gene: KIF6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39340966A>G , CM000668.2:g.39340966A>G GRCh38
NC_000006.11:g.39308742A>G , CM000668.1:g.39308742A>G GRCh37
NC_000006.10:g.39416720A>G NCBI36
NG_054928.1:g.389459T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000287152.12:c.2428+2743T>C MANE Select ENSP00000287152.7:n.2428+2743T>C
ENST00000229913.9:c.781+2743T>C ENSP00000229913.5:n.781+2743T>C
ENST00000287152.11:c.2428+2743T>C ENSP00000287152.7:n.2428+2743T>C
ENST00000394362.5:c.730+2743T>C ENSP00000377889.1:n.730+2743T>C
ENST00000458470.5:c.2052+2743T>C
NM_001289020.1:c.2377+2743T>C NP_001275949.1:n.2377+2743T>C
NM_001289021.1:c.2260+2743T>C NP_001275950.1:n.2260+2743T>C
NM_001289024.1:c.781+2743T>C NP_001275953.1:n.781+2743T>C
NM_145027.4:c.2428+2743T>C NP_659464.3:n.2428+2743T>C
XM_011514359.1:c.2377+2743T>C XP_011512661.1:n.2377+2743T>C
XR_926774.1:n.239-1673A>G
NM_001289020.2:c.2377+2743T>C NP_001275949.1:n.2377+2743T>C
NM_001289021.2:c.2260+2743T>C NP_001275950.1:n.2260+2743T>C
NM_001289024.2:c.781+2743T>C NP_001275953.1:n.781+2743T>C
NM_145027.5:c.2428+2743T>C NP_659464.3:n.2428+2743T>C
XM_011514359.3:c.2377+2743T>C XP_011512661.1:n.2377+2743T>C
XR_926774.2:n.249-1673A>G
NM_145027.6:c.2428+2743T>C MANE Select NP_659464.3:n.2428+2743T>C
NM_001289020.3:c.2377+2743T>C NP_001275949.1:n.2377+2743T>C
NM_001289021.3:c.2260+2743T>C NP_001275950.1:n.2260+2743T>C
NM_001289024.3:c.781+2743T>C NP_001275953.1:n.781+2743T>C
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