Canonical Allele Identifier: CA2687151981

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43193734-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43193735_43193736del , CM000670.2:g.43193735_43193736del	GRCh38
NC_000008.10:g.43048878_43048879del , CM000670.1:g.43048878_43048879del	GRCh37
NC_000008.9:g.43168035_43168036del	NCBI36
NG_009552.1:g.58287_58288del

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1378-22_1378-21del MANE Select	ENSP00000368965.4:n.1378-22_1378-21del
ENST00000379644.8:c.1378-22_1378-21del	ENSP00000368965.4:n.1378-22_1378-21del
ENST00000520678.1:n.311-22_311-21del
ENST00000521576.1:c.529-22_529-21del	ENSP00000429029.1:n.529-22_529-21del
ENST00000524016.5:c.482-22_482-21del
NM_152419.2:c.1378-22_1378-21del	NP_689632.2:n.1378-22_1378-21del
XM_005273409.1:c.1378-22_1378-21del	XP_005273466.1:n.1378-22_1378-21del
XM_005273410.1:c.1378-22_1378-21del	XP_005273467.1:n.1378-22_1378-21del
XM_005273411.1:c.1186-22_1186-21del	XP_005273468.1:n.1186-22_1186-21del
XM_005273412.2:c.1378-22_1378-21del	XP_005273469.1:n.1378-22_1378-21del
NM_001363227.1:c.1378-22_1378-21del	NP_001350156.1:n.1378-22_1378-21del
NM_001363228.1:c.1186-22_1186-21del	NP_001350157.1:n.1186-22_1186-21del
NM_001363229.1:c.514-22_514-21del	NP_001350158.1:n.514-22_514-21del
XM_005273412.4:c.1378-22_1378-21del	XP_005273469.1:n.1378-22_1378-21del
NM_152419.3:c.1378-22_1378-21del MANE Select	NP_689632.2:n.1378-22_1378-21del
NM_001363227.2:c.1378-22_1378-21del	NP_001350156.1:n.1378-22_1378-21del
NM_001363228.2:c.1186-22_1186-21del	NP_001350157.1:n.1186-22_1186-21del
NM_001363229.2:c.514-22_514-21del	NP_001350158.1:n.514-22_514-21del