Canonical Allele Identifier: CA11326100
Gene: FTCDNL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.199773786T>G , CM000664.2:g.199773786T>G GRCh38
NC_000002.11:g.200638509T>G , CM000664.1:g.200638509T>G GRCh37
NC_000002.10:g.200346754T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000416668.5:c.212-12951A>C ENSP00000454447.1:n.212-12951A>C
ENST00000420922.6:c.*20-12951A>C ENSP00000456442.1:n.*20-12951A>C
NR_034096.1:n.653-12951A>C
NM_001350854.1:c.*20-12951A>C NP_001337783.1:n.*20-12951A>C
NM_001350855.1:c.212-12951A>C NP_001337784.1:n.212-12951A>C
XM_024452852.1:c.397+45786A>C XP_024308620.1:n.397+45786A>C
XM_024452853.1:c.397+45786A>C XP_024308621.1:n.397+45786A>C
XM_024452855.1:c.398-12951A>C XP_024308623.1:n.398-12951A>C
XM_024452858.1:c.212-10114A>C XP_024308626.1:n.212-10114A>C
XM_024452861.1:c.*20-12951A>C XP_024308629.1:n.*20-12951A>C
XM_024452863.1:c.211+72289A>C XP_024308631.1:n.211+72289A>C
XM_024452864.1:c.211+72289A>C XP_024308632.1:n.211+72289A>C
XM_024452865.1:c.211+72289A>C XP_024308633.1:n.211+72289A>C
XM_024452867.1:c.*1875A>C XP_024308635.1:n.*1875A>C
XM_024452868.1:c.211+72289A>C XP_024308636.1:n.211+72289A>C
XM_024452869.1:c.212-12951A>C XP_024308637.1:n.212-12951A>C
XM_024452871.1:c.397+45786A>C XP_024308639.1:n.397+45786A>C
XR_002959289.1:n.2581A>C
NM_001350854.2:c.*20-12951A>C NP_001337783.1:n.*20-12951A>C
NM_001350855.2:c.212-12951A>C NP_001337784.1:n.212-12951A>C
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