Canonical Allele Identifier: CA1241978363

Gene: GALNT14

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31074695G= , CM000664.2:g.31074695G=	GRCh38
NC_000002.11:g.31297561G= , CM000664.1:g.31297561G=	GRCh37
NC_000002.10:g.31151065G=	NCBI36
NG_051040.1:g.69032C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000349752.10:c.129+63263C= MANE Select	ENSP00000288988.6:n.129+63263C=
ENST00000324589.9:c.314+40048C=	ENSP00000314500.5:n.314+40048C=
ENST00000349752.9:c.129+63263C=	ENSP00000288988.6:n.129+63263C=
ENST00000406653.5:c.69+40048C=	ENSP00000385435.1:n.69+40048C=
ENST00000424136.5:c.181+57935C=
ENST00000430167.1:c.129+63263C=	ENSP00000406399.1:n.129+63263C=
ENST00000455477.5:c.198+50459C=
ENST00000461193.5:n.164+50459C=
ENST00000464038.5:n.388+72227C=
ENST00000485468.1:n.290+4239C=
ENST00000490212.5:n.364+54582C=
ENST00000496397.5:n.202-1520C=
ENST00000498206.5:n.358+40048C=
NM_001253826.1:c.314+40048C=	NP_001240755.1:n.314+40048C=
NM_001253827.1:c.69+40048C=	NP_001240756.1:n.69+40048C=
NM_024572.3:c.129+63263C=	NP_078848.2:n.129+63263C=
NR_045602.1:n.902+4239C=
XM_011533104.1:c.447+4239C=	XP_011531406.1:n.447+4239C=
XM_011533105.1:c.69+40048C=	XP_011531407.1:n.69+40048C=
XM_011533106.1:c.42+72227C=	XP_011531408.1:n.42+72227C=
NM_001329095.1:c.24+4239C=	NP_001316024.1:n.24+4239C=
NM_001329096.1:c.69+40048C=	NP_001316025.1:n.69+40048C=
NM_001329097.1:c.129+63263C=	NP_001316026.1:n.129+63263C=
XM_017004906.1:c.162+4239C=	XP_016860395.1:n.162+4239C=
XM_017004907.1:c.162+4239C=	XP_016860396.1:n.162+4239C=
XR_001738941.1:n.236+4239C=
XR_001738942.1:n.236+4239C=
XR_001738943.1:n.245+4239C=
NM_024572.4:c.129+63263C= MANE Select	NP_078848.2:n.129+63263C=
NM_001253826.2:c.314+40048C=	NP_001240755.1:n.314+40048C=
NM_001329095.2:c.24+4239C=	NP_001316024.1:n.24+4239C=
NM_001329096.2:c.69+40048C=	NP_001316025.1:n.69+40048C=
NM_001329097.2:c.129+63263C=	NP_001316026.1:n.129+63263C=
NM_001253827.2:c.69+40048C=	NP_001240756.1:n.69+40048C=