Canonical Allele Identifier: CA1241978386

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31074746_31074748delinsCAT , CM000664.2:g.31074746_31074748delinsCAT	GRCh38
NC_000002.11:g.31297612_31297614delinsCAT , CM000664.1:g.31297612_31297614delinsCAT	GRCh37
NC_000002.10:g.31151116_31151118delinsCAT	NCBI36
NG_051040.1:g.68979_68981delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+63210_129+63212delinsATG MANE Select	ENSP00000288988.6:n.129+63210_129+63212delinsATG
ENST00000324589.9:c.314+39995_314+39997delinsATG	ENSP00000314500.5:n.314+39995_314+39997delinsATG
ENST00000349752.9:c.129+63210_129+63212delinsATG	ENSP00000288988.6:n.129+63210_129+63212delinsATG
ENST00000406653.5:c.69+39995_69+39997delinsATG	ENSP00000385435.1:n.69+39995_69+39997delinsATG
ENST00000424136.5:c.181+57882_181+57884delinsATG
ENST00000430167.1:c.129+63210_129+63212delinsATG	ENSP00000406399.1:n.129+63210_129+63212delinsATG
ENST00000455477.5:c.198+50406_198+50408delinsATG
ENST00000461193.5:n.164+50406_164+50408delinsATG
ENST00000464038.5:n.388+72174_388+72176delinsATG
ENST00000485468.1:n.290+4186_290+4188delinsATG
ENST00000490212.5:n.364+54529_364+54531delinsATG
ENST00000496397.5:n.202-1573_202-1571delinsATG
ENST00000498206.5:n.358+39995_358+39997delinsATG
NM_001253826.1:c.314+39995_314+39997delinsATG	NP_001240755.1:n.314+39995_314+39997delinsATG
NM_001253827.1:c.69+39995_69+39997delinsATG	NP_001240756.1:n.69+39995_69+39997delinsATG
NM_024572.3:c.129+63210_129+63212delinsATG	NP_078848.2:n.129+63210_129+63212delinsATG
NR_045602.1:n.902+4186_902+4188delinsATG
XM_011533104.1:c.447+4186_447+4188delinsATG	XP_011531406.1:n.447+4186_447+4188delinsATG
XM_011533105.1:c.69+39995_69+39997delinsATG	XP_011531407.1:n.69+39995_69+39997delinsATG
XM_011533106.1:c.42+72174_42+72176delinsATG	XP_011531408.1:n.42+72174_42+72176delinsATG
NM_001329095.1:c.24+4186_24+4188delinsATG	NP_001316024.1:n.24+4186_24+4188delinsATG
NM_001329096.1:c.69+39995_69+39997delinsATG	NP_001316025.1:n.69+39995_69+39997delinsATG
NM_001329097.1:c.129+63210_129+63212delinsATG	NP_001316026.1:n.129+63210_129+63212delinsATG
XM_017004906.1:c.162+4186_162+4188delinsATG	XP_016860395.1:n.162+4186_162+4188delinsATG
XM_017004907.1:c.162+4186_162+4188delinsATG	XP_016860396.1:n.162+4186_162+4188delinsATG
XR_001738941.1:n.236+4186_236+4188delinsATG
XR_001738942.1:n.236+4186_236+4188delinsATG
XR_001738943.1:n.245+4186_245+4188delinsATG
NM_024572.4:c.129+63210_129+63212delinsATG MANE Select	NP_078848.2:n.129+63210_129+63212delinsATG
NM_001253826.2:c.314+39995_314+39997delinsATG	NP_001240755.1:n.314+39995_314+39997delinsATG
NM_001329095.2:c.24+4186_24+4188delinsATG	NP_001316024.1:n.24+4186_24+4188delinsATG
NM_001329096.2:c.69+39995_69+39997delinsATG	NP_001316025.1:n.69+39995_69+39997delinsATG
NM_001329097.2:c.129+63210_129+63212delinsATG	NP_001316026.1:n.129+63210_129+63212delinsATG
NM_001253827.2:c.69+39995_69+39997delinsATG	NP_001240756.1:n.69+39995_69+39997delinsATG