Canonical Allele Identifier: CA2687151440

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43192169-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192170_43192171del , CM000670.2:g.43192170_43192171del	GRCh38
NC_000008.10:g.43047313_43047314del , CM000670.1:g.43047313_43047314del	GRCh37
NC_000008.9:g.43166470_43166471del	NCBI36
NG_009552.1:g.56722_56723del

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1251-134_1251-133del MANE Select	ENSP00000368965.4:n.1251-134_1251-133del
ENST00000379644.8:c.1251-134_1251-133del	ENSP00000368965.4:n.1251-134_1251-133del
ENST00000520678.1:n.184-134_184-133del
ENST00000521576.1:c.402-134_402-133del	ENSP00000429029.1:n.402-134_402-133del
ENST00000524016.5:c.355-134_355-133del
NM_152419.2:c.1251-134_1251-133del	NP_689632.2:n.1251-134_1251-133del
XM_005273409.1:c.1251-134_1251-133del	XP_005273466.1:n.1251-134_1251-133del
XM_005273410.1:c.1251-134_1251-133del	XP_005273467.1:n.1251-134_1251-133del
XM_005273411.1:c.1059-134_1059-133del	XP_005273468.1:n.1059-134_1059-133del
XM_005273412.2:c.1251-134_1251-133del	XP_005273469.1:n.1251-134_1251-133del
NM_001363227.1:c.1251-134_1251-133del	NP_001350156.1:n.1251-134_1251-133del
NM_001363228.1:c.1059-134_1059-133del	NP_001350157.1:n.1059-134_1059-133del
NM_001363229.1:c.387-134_387-133del	NP_001350158.1:n.387-134_387-133del
XM_005273412.4:c.1251-134_1251-133del	XP_005273469.1:n.1251-134_1251-133del
NM_152419.3:c.1251-134_1251-133del MANE Select	NP_689632.2:n.1251-134_1251-133del
NM_001363227.2:c.1251-134_1251-133del	NP_001350156.1:n.1251-134_1251-133del
NM_001363228.2:c.1059-134_1059-133del	NP_001350157.1:n.1059-134_1059-133del
NM_001363229.2:c.387-134_387-133del	NP_001350158.1:n.387-134_387-133del