Canonical Allele Identifier: CA1241986422

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31091686_31091687delinsGT , CM000664.2:g.31091686_31091687delinsGT	GRCh38
NC_000002.11:g.31314552_31314553delinsGT , CM000664.1:g.31314552_31314553delinsGT	GRCh37
NC_000002.10:g.31168056_31168057delinsGT	NCBI36
NG_051040.1:g.52040_52041delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+46271_129+46272delinsAC MANE Select	ENSP00000288988.6:n.129+46271_129+46272delinsAC
ENST00000324589.9:c.314+23056_314+23057delinsAC	ENSP00000314500.5:n.314+23056_314+23057delinsAC
ENST00000349752.9:c.129+46271_129+46272delinsAC	ENSP00000288988.6:n.129+46271_129+46272delinsAC
ENST00000406653.5:c.69+23056_69+23057delinsAC	ENSP00000385435.1:n.69+23056_69+23057delinsAC
ENST00000424136.5:c.181+40943_181+40944delinsAC
ENST00000430167.1:c.129+46271_129+46272delinsAC	ENSP00000406399.1:n.129+46271_129+46272delinsAC
ENST00000455477.5:c.198+33467_198+33468delinsAC
ENST00000461193.5:n.164+33467_164+33468delinsAC
ENST00000464038.5:n.388+55235_388+55236delinsAC
ENST00000485468.1:n.158-12621_158-12620delinsAC
ENST00000490212.5:n.364+37590_364+37591delinsAC
ENST00000496397.5:n.202-18512_202-18511delinsAC
ENST00000498206.5:n.358+23056_358+23057delinsAC
NM_001253826.1:c.314+23056_314+23057delinsAC	NP_001240755.1:n.314+23056_314+23057delinsAC
NM_001253827.1:c.69+23056_69+23057delinsAC	NP_001240756.1:n.69+23056_69+23057delinsAC
NM_024572.3:c.129+46271_129+46272delinsAC	NP_078848.2:n.129+46271_129+46272delinsAC
NR_045602.1:n.770-12621_770-12620delinsAC
XM_011533104.1:c.315-12621_315-12620delinsAC	XP_011531406.1:n.315-12621_315-12620delinsAC
XM_011533105.1:c.69+23056_69+23057delinsAC	XP_011531407.1:n.69+23056_69+23057delinsAC
XM_011533106.1:c.42+55235_42+55236delinsAC	XP_011531408.1:n.42+55235_42+55236delinsAC
NM_001329095.1:c.-109-12621_-109-12620delinsAC	NP_001316024.1:n.-109-12621_-109-12620delinsAC
NM_001329096.1:c.69+23056_69+23057delinsAC	NP_001316025.1:n.69+23056_69+23057delinsAC
NM_001329097.1:c.129+46271_129+46272delinsAC	NP_001316026.1:n.129+46271_129+46272delinsAC
NM_024572.4:c.129+46271_129+46272delinsAC MANE Select	NP_078848.2:n.129+46271_129+46272delinsAC
NM_001253826.2:c.314+23056_314+23057delinsAC	NP_001240755.1:n.314+23056_314+23057delinsAC
NM_001329095.2:c.-109-12621_-109-12620delinsAC	NP_001316024.1:n.-109-12621_-109-12620delinsAC
NM_001329096.2:c.69+23056_69+23057delinsAC	NP_001316025.1:n.69+23056_69+23057delinsAC
NM_001329097.2:c.129+46271_129+46272delinsAC	NP_001316026.1:n.129+46271_129+46272delinsAC
NM_001253827.2:c.69+23056_69+23057delinsAC	NP_001240756.1:n.69+23056_69+23057delinsAC