Canonical Allele Identifier: CA11135029
Gene: FTCDNL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.199812203A>C , CM000664.2:g.199812203A>C GRCh38
NC_000002.11:g.200676926A>C , CM000664.1:g.200676926A>C GRCh37
NC_000002.10:g.200385171A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420128.6:c.*502T>G MANE Select ENSP00000457780.1:n.*502T>G
ENST00000642693.1:n.405+7369T>G
ENST00000416668.5:c.211+33872T>G ENSP00000454447.1:n.211+33872T>G
ENST00000420922.6:c.*19+32177T>G ENSP00000456442.1:n.*19+32177T>G
NR_034096.1:n.652+33872T>G
XR_923761.1:n.560T>G
NM_001350854.1:c.*19+32177T>G NP_001337783.1:n.*19+32177T>G
NM_001350855.1:c.211+33872T>G NP_001337784.1:n.211+33872T>G
NM_001363886.1:c.*502T>G NP_001350815.1:n.*502T>G
XM_024452852.1:c.397+7369T>G XP_024308620.1:n.397+7369T>G
XM_024452853.1:c.397+7369T>G XP_024308621.1:n.397+7369T>G
XM_024452854.1:c.397+7369T>G XP_024308622.1:n.397+7369T>G
XM_024452855.1:c.397+7369T>G XP_024308623.1:n.397+7369T>G
XM_024452857.1:c.398-4944T>G XP_024308625.1:n.398-4944T>G
XM_024452858.1:c.211+33872T>G XP_024308626.1:n.211+33872T>G
XM_024452861.1:c.*19+32177T>G XP_024308629.1:n.*19+32177T>G
XM_024452863.1:c.211+33872T>G XP_024308631.1:n.211+33872T>G
XM_024452864.1:c.211+33872T>G XP_024308632.1:n.211+33872T>G
XM_024452865.1:c.211+33872T>G XP_024308633.1:n.211+33872T>G
XM_024452866.1:c.212-28360T>G XP_024308634.1:n.212-28360T>G
XM_024452867.1:c.211+33872T>G XP_024308635.1:n.211+33872T>G
XM_024452868.1:c.211+33872T>G XP_024308636.1:n.211+33872T>G
XM_024452869.1:c.211+33872T>G XP_024308637.1:n.211+33872T>G
XM_024452870.1:c.*502T>G XP_024308638.1:n.*502T>G
XM_024452871.1:c.397+7369T>G XP_024308639.1:n.397+7369T>G
XM_024452872.1:c.212-26625T>G XP_024308640.1:n.212-26625T>G
XR_002959288.1:n.858+365T>G
XR_002959289.1:n.516-28360T>G
NM_001350854.2:c.*19+32177T>G NP_001337783.1:n.*19+32177T>G
NM_001350855.2:c.211+33872T>G NP_001337784.1:n.211+33872T>G
NM_001363886.2:c.*502T>G MANE Select NP_001350815.1:n.*502T>G
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