Canonical Allele Identifier: CA2698776356

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.30993531G>T , CM000664.2:g.30993531G>T	GRCh38
NC_000002.11:g.31216397G>T , CM000664.1:g.31216397G>T	GRCh37
NC_000002.10:g.31069901G>T	NCBI36
NG_051040.1:g.150196C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024572.4:c.130-524C>A MANE Select	NP_078848.2:n.130-524C>A
ENST00000349752.10:c.130-524C>A MANE Select	ENSP00000288988.6:n.130-524C>A
NM_001253826.1:c.315-27229C>A	NP_001240755.1:n.315-27229C>A
NM_001253826.2:c.315-27229C>A	NP_001240755.1:n.315-27229C>A
NM_001253827.1:c.70-524C>A	NP_001240756.1:n.70-524C>A
NM_001253827.2:c.70-524C>A	NP_001240756.1:n.70-524C>A
NM_001329095.1:c.25-524C>A	NP_001316024.1:n.25-524C>A
NM_001329095.2:c.25-524C>A	NP_001316024.1:n.25-524C>A
NM_001329096.1:c.70-524C>A	NP_001316025.1:n.70-524C>A
NM_001329096.2:c.70-524C>A	NP_001316025.1:n.70-524C>A
NM_001329097.1:c.130-524C>A	NP_001316026.1:n.130-524C>A
NM_001329097.2:c.130-524C>A	NP_001316026.1:n.130-524C>A
NM_024572.3:c.130-524C>A	NP_078848.2:n.130-524C>A
NR_045602.1:n.903-524C>A
ENST00000324589.9:c.315-27229C>A	ENSP00000314500.5:n.315-27229C>A
ENST00000349752.9:c.130-524C>A	ENSP00000288988.6:n.130-524C>A
ENST00000406653.5:c.70-524C>A	ENSP00000385435.1:n.70-524C>A
ENST00000424136.5:c.182-524C>A
ENST00000430167.1:c.130-524C>A	ENSP00000406399.1:n.130-524C>A
ENST00000455477.5:c.199-524C>A
ENST00000461193.5:n.165-524C>A
ENST00000464038.5:n.389-524C>A
ENST00000490212.5:n.365-524C>A
ENST00000496397.5:n.315-524C>A
ENST00000498206.5:n.359-524C>A
XM_011533104.1:c.448-524C>A	XP_011531406.1:n.448-524C>A
XM_011533105.1:c.70-524C>A	XP_011531407.1:n.70-524C>A
XM_011533106.1:c.43-524C>A	XP_011531408.1:n.43-524C>A
XM_017004906.1:c.163-524C>A	XP_016860395.1:n.163-524C>A
XM_017004907.1:c.163-524C>A	XP_016860396.1:n.163-524C>A
XR_001738941.1:n.237-524C>A
XR_001738942.1:n.237-524C>A
XR_001738943.1:n.246-524C>A