Canonical Allele Identifier: CA2749362745

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31074422_31074423insTTT , CM000664.2:g.31074422_31074423insTTT	GRCh38
NC_000002.11:g.31297288_31297289insTTT , CM000664.1:g.31297288_31297289insTTT	GRCh37
NC_000002.10:g.31150792_31150793insTTT	NCBI36
NG_051040.1:g.69306_69307insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+63537_129+63538insAAA MANE Select	ENSP00000288988.6:n.129+63537_129+63538insAAA
ENST00000324589.9:c.314+40322_314+40323insAAA	ENSP00000314500.5:n.314+40322_314+40323insAAA
ENST00000349752.9:c.129+63537_129+63538insAAA	ENSP00000288988.6:n.129+63537_129+63538insAAA
ENST00000406653.5:c.69+40322_69+40323insAAA	ENSP00000385435.1:n.69+40322_69+40323insAAA
ENST00000424136.5:c.181+58209_181+58210insAAA
ENST00000430167.1:c.129+63537_129+63538insAAA	ENSP00000406399.1:n.129+63537_129+63538insAAA
ENST00000455477.5:c.198+50733_198+50734insAAA
ENST00000461193.5:n.164+50733_164+50734insAAA
ENST00000464038.5:n.388+72501_388+72502insAAA
ENST00000485468.1:n.290+4513_290+4514insAAA
ENST00000490212.5:n.364+54856_364+54857insAAA
ENST00000496397.5:n.202-1246_202-1245insAAA
ENST00000498206.5:n.358+40322_358+40323insAAA
NM_001253826.1:c.314+40322_314+40323insAAA	NP_001240755.1:n.314+40322_314+40323insAAA
NM_001253827.1:c.69+40322_69+40323insAAA	NP_001240756.1:n.69+40322_69+40323insAAA
NM_024572.3:c.129+63537_129+63538insAAA	NP_078848.2:n.129+63537_129+63538insAAA
NR_045602.1:n.902+4513_902+4514insAAA
XM_011533104.1:c.447+4513_447+4514insAAA	XP_011531406.1:n.447+4513_447+4514insAAA
XM_011533105.1:c.69+40322_69+40323insAAA	XP_011531407.1:n.69+40322_69+40323insAAA
XM_011533106.1:c.42+72501_42+72502insAAA	XP_011531408.1:n.42+72501_42+72502insAAA
NM_001329095.1:c.24+4513_24+4514insAAA	NP_001316024.1:n.24+4513_24+4514insAAA
NM_001329096.1:c.69+40322_69+40323insAAA	NP_001316025.1:n.69+40322_69+40323insAAA
NM_001329097.1:c.129+63537_129+63538insAAA	NP_001316026.1:n.129+63537_129+63538insAAA
XM_017004906.1:c.162+4513_162+4514insAAA	XP_016860395.1:n.162+4513_162+4514insAAA
XM_017004907.1:c.162+4513_162+4514insAAA	XP_016860396.1:n.162+4513_162+4514insAAA
XR_001738941.1:n.236+4513_236+4514insAAA
XR_001738942.1:n.236+4513_236+4514insAAA
XR_001738943.1:n.245+4513_245+4514insAAA
NM_024572.4:c.129+63537_129+63538insAAA MANE Select	NP_078848.2:n.129+63537_129+63538insAAA
NM_001253826.2:c.314+40322_314+40323insAAA	NP_001240755.1:n.314+40322_314+40323insAAA
NM_001329095.2:c.24+4513_24+4514insAAA	NP_001316024.1:n.24+4513_24+4514insAAA
NM_001329096.2:c.69+40322_69+40323insAAA	NP_001316025.1:n.69+40322_69+40323insAAA
NM_001329097.2:c.129+63537_129+63538insAAA	NP_001316026.1:n.129+63537_129+63538insAAA
NM_001253827.2:c.69+40322_69+40323insAAA	NP_001240756.1:n.69+40322_69+40323insAAA