Canonical Allele Identifier: CA1241978392

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31074763A= , CM000664.2:g.31074763A=	GRCh38
NC_000002.11:g.31297629A= , CM000664.1:g.31297629A=	GRCh37
NC_000002.10:g.31151133A=	NCBI36
NG_051040.1:g.68964T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349752.10:c.129+63195T= MANE Select	ENSP00000288988.6:n.129+63195T=
ENST00000324589.9:c.314+39980T=	ENSP00000314500.5:n.314+39980T=
ENST00000349752.9:c.129+63195T=	ENSP00000288988.6:n.129+63195T=
ENST00000406653.5:c.69+39980T=	ENSP00000385435.1:n.69+39980T=
ENST00000424136.5:c.181+57867T=
ENST00000430167.1:c.129+63195T=	ENSP00000406399.1:n.129+63195T=
ENST00000455477.5:c.198+50391T=
ENST00000461193.5:n.164+50391T=
ENST00000464038.5:n.388+72159T=
ENST00000485468.1:n.290+4171T=
ENST00000490212.5:n.364+54514T=
ENST00000496397.5:n.202-1588T=
ENST00000498206.5:n.358+39980T=
NM_001253826.1:c.314+39980T=	NP_001240755.1:n.314+39980T=
NM_001253827.1:c.69+39980T=	NP_001240756.1:n.69+39980T=
NM_024572.3:c.129+63195T=	NP_078848.2:n.129+63195T=
NR_045602.1:n.902+4171T=
XM_011533104.1:c.447+4171T=	XP_011531406.1:n.447+4171T=
XM_011533105.1:c.69+39980T=	XP_011531407.1:n.69+39980T=
XM_011533106.1:c.42+72159T=	XP_011531408.1:n.42+72159T=
NM_001329095.1:c.24+4171T=	NP_001316024.1:n.24+4171T=
NM_001329096.1:c.69+39980T=	NP_001316025.1:n.69+39980T=
NM_001329097.1:c.129+63195T=	NP_001316026.1:n.129+63195T=
XM_017004906.1:c.162+4171T=	XP_016860395.1:n.162+4171T=
XM_017004907.1:c.162+4171T=	XP_016860396.1:n.162+4171T=
XR_001738941.1:n.236+4171T=
XR_001738942.1:n.236+4171T=
XR_001738943.1:n.245+4171T=
NM_024572.4:c.129+63195T= MANE Select	NP_078848.2:n.129+63195T=
NM_001253826.2:c.314+39980T=	NP_001240755.1:n.314+39980T=
NM_001329095.2:c.24+4171T=	NP_001316024.1:n.24+4171T=
NM_001329096.2:c.69+39980T=	NP_001316025.1:n.69+39980T=
NM_001329097.2:c.129+63195T=	NP_001316026.1:n.129+63195T=
NM_001253827.2:c.69+39980T=	NP_001240756.1:n.69+39980T=