Canonical Allele Identifier: CA1241978362

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31074694_31074698delinsGGAGA , CM000664.2:g.31074694_31074698delinsGGAGA	GRCh38
NC_000002.11:g.31297560_31297564delinsGGAGA , CM000664.1:g.31297560_31297564delinsGGAGA	GRCh37
NC_000002.10:g.31151064_31151068delinsGGAGA	NCBI36
NG_051040.1:g.69029_69033delinsTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+63260_129+63264delinsTCTCC MANE Select	ENSP00000288988.6:n.129+63260_129+63264delinsTCTCC
ENST00000324589.9:c.314+40045_314+40049delinsTCTCC	ENSP00000314500.5:n.314+40045_314+40049delinsTCTCC
ENST00000349752.9:c.129+63260_129+63264delinsTCTCC	ENSP00000288988.6:n.129+63260_129+63264delinsTCTCC
ENST00000406653.5:c.69+40045_69+40049delinsTCTCC	ENSP00000385435.1:n.69+40045_69+40049delinsTCTCC
ENST00000424136.5:c.181+57932_181+57936delinsTCTCC
ENST00000430167.1:c.129+63260_129+63264delinsTCTCC	ENSP00000406399.1:n.129+63260_129+63264delinsTCTCC
ENST00000455477.5:c.198+50456_198+50460delinsTCTCC
ENST00000461193.5:n.164+50456_164+50460delinsTCTCC
ENST00000464038.5:n.388+72224_388+72228delinsTCTCC
ENST00000485468.1:n.290+4236_290+4240delinsTCTCC
ENST00000490212.5:n.364+54579_364+54583delinsTCTCC
ENST00000496397.5:n.202-1523_202-1519delinsTCTCC
ENST00000498206.5:n.358+40045_358+40049delinsTCTCC
NM_001253826.1:c.314+40045_314+40049delinsTCTCC	NP_001240755.1:n.314+40045_314+40049delinsTCTCC
NM_001253827.1:c.69+40045_69+40049delinsTCTCC	NP_001240756.1:n.69+40045_69+40049delinsTCTCC
NM_024572.3:c.129+63260_129+63264delinsTCTCC	NP_078848.2:n.129+63260_129+63264delinsTCTCC
NR_045602.1:n.902+4236_902+4240delinsTCTCC
XM_011533104.1:c.447+4236_447+4240delinsTCTCC	XP_011531406.1:n.447+4236_447+4240delinsTCTCC
XM_011533105.1:c.69+40045_69+40049delinsTCTCC	XP_011531407.1:n.69+40045_69+40049delinsTCTCC
XM_011533106.1:c.42+72224_42+72228delinsTCTCC	XP_011531408.1:n.42+72224_42+72228delinsTCTCC
NM_001329095.1:c.24+4236_24+4240delinsTCTCC	NP_001316024.1:n.24+4236_24+4240delinsTCTCC
NM_001329096.1:c.69+40045_69+40049delinsTCTCC	NP_001316025.1:n.69+40045_69+40049delinsTCTCC
NM_001329097.1:c.129+63260_129+63264delinsTCTCC	NP_001316026.1:n.129+63260_129+63264delinsTCTCC
XM_017004906.1:c.162+4236_162+4240delinsTCTCC	XP_016860395.1:n.162+4236_162+4240delinsTCTCC
XM_017004907.1:c.162+4236_162+4240delinsTCTCC	XP_016860396.1:n.162+4236_162+4240delinsTCTCC
XR_001738941.1:n.236+4236_236+4240delinsTCTCC
XR_001738942.1:n.236+4236_236+4240delinsTCTCC
XR_001738943.1:n.245+4236_245+4240delinsTCTCC
NM_024572.4:c.129+63260_129+63264delinsTCTCC MANE Select	NP_078848.2:n.129+63260_129+63264delinsTCTCC
NM_001253826.2:c.314+40045_314+40049delinsTCTCC	NP_001240755.1:n.314+40045_314+40049delinsTCTCC
NM_001329095.2:c.24+4236_24+4240delinsTCTCC	NP_001316024.1:n.24+4236_24+4240delinsTCTCC
NM_001329096.2:c.69+40045_69+40049delinsTCTCC	NP_001316025.1:n.69+40045_69+40049delinsTCTCC
NM_001329097.2:c.129+63260_129+63264delinsTCTCC	NP_001316026.1:n.129+63260_129+63264delinsTCTCC
NM_001253827.2:c.69+40045_69+40049delinsTCTCC	NP_001240756.1:n.69+40045_69+40049delinsTCTCC