Canonical Allele Identifier: CA1241978353
Gene: GALNT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31074681_31074685delinsAAAAG , CM000664.2:g.31074681_31074685delinsAAAAG GRCh38
NC_000002.11:g.31297547_31297551delinsAAAAG , CM000664.1:g.31297547_31297551delinsAAAAG GRCh37
NC_000002.10:g.31151051_31151055delinsAAAAG NCBI36
NG_051040.1:g.69042_69046delinsCTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000349752.10:c.129+63273_129+63277delinsCTTTT MANE Select ENSP00000288988.6:n.129+63273_129+63277delinsCTTTT
ENST00000324589.9:c.314+40058_314+40062delinsCTTTT ENSP00000314500.5:n.314+40058_314+40062delinsCTTTT
ENST00000349752.9:c.129+63273_129+63277delinsCTTTT ENSP00000288988.6:n.129+63273_129+63277delinsCTTTT
ENST00000406653.5:c.69+40058_69+40062delinsCTTTT ENSP00000385435.1:n.69+40058_69+40062delinsCTTTT
ENST00000424136.5:c.181+57945_181+57949delinsCTTTT
ENST00000430167.1:c.129+63273_129+63277delinsCTTTT ENSP00000406399.1:n.129+63273_129+63277delinsCTTTT
ENST00000455477.5:c.198+50469_198+50473delinsCTTTT
ENST00000461193.5:n.164+50469_164+50473delinsCTTTT
ENST00000464038.5:n.388+72237_388+72241delinsCTTTT
ENST00000485468.1:n.290+4249_290+4253delinsCTTTT
ENST00000490212.5:n.364+54592_364+54596delinsCTTTT
ENST00000496397.5:n.202-1510_202-1506delinsCTTTT
ENST00000498206.5:n.358+40058_358+40062delinsCTTTT
NM_001253826.1:c.314+40058_314+40062delinsCTTTT NP_001240755.1:n.314+40058_314+40062delinsCTTTT
NM_001253827.1:c.69+40058_69+40062delinsCTTTT NP_001240756.1:n.69+40058_69+40062delinsCTTTT
NM_024572.3:c.129+63273_129+63277delinsCTTTT NP_078848.2:n.129+63273_129+63277delinsCTTTT
NR_045602.1:n.902+4249_902+4253delinsCTTTT
XM_011533104.1:c.447+4249_447+4253delinsCTTTT XP_011531406.1:n.447+4249_447+4253delinsCTTTT
XM_011533105.1:c.69+40058_69+40062delinsCTTTT XP_011531407.1:n.69+40058_69+40062delinsCTTTT
XM_011533106.1:c.42+72237_42+72241delinsCTTTT XP_011531408.1:n.42+72237_42+72241delinsCTTTT
NM_001329095.1:c.24+4249_24+4253delinsCTTTT NP_001316024.1:n.24+4249_24+4253delinsCTTTT
NM_001329096.1:c.69+40058_69+40062delinsCTTTT NP_001316025.1:n.69+40058_69+40062delinsCTTTT
NM_001329097.1:c.129+63273_129+63277delinsCTTTT NP_001316026.1:n.129+63273_129+63277delinsCTTTT
XM_017004906.1:c.162+4249_162+4253delinsCTTTT XP_016860395.1:n.162+4249_162+4253delinsCTTTT
XM_017004907.1:c.162+4249_162+4253delinsCTTTT XP_016860396.1:n.162+4249_162+4253delinsCTTTT
XR_001738941.1:n.236+4249_236+4253delinsCTTTT
XR_001738942.1:n.236+4249_236+4253delinsCTTTT
XR_001738943.1:n.245+4249_245+4253delinsCTTTT
NM_024572.4:c.129+63273_129+63277delinsCTTTT MANE Select NP_078848.2:n.129+63273_129+63277delinsCTTTT
NM_001253826.2:c.314+40058_314+40062delinsCTTTT NP_001240755.1:n.314+40058_314+40062delinsCTTTT
NM_001329095.2:c.24+4249_24+4253delinsCTTTT NP_001316024.1:n.24+4249_24+4253delinsCTTTT
NM_001329096.2:c.69+40058_69+40062delinsCTTTT NP_001316025.1:n.69+40058_69+40062delinsCTTTT
NM_001329097.2:c.129+63273_129+63277delinsCTTTT NP_001316026.1:n.129+63273_129+63277delinsCTTTT
NM_001253827.2:c.69+40058_69+40062delinsCTTTT NP_001240756.1:n.69+40058_69+40062delinsCTTTT