Canonical Allele Identifier: CA2687154310

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43197620-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197620T>C , CM000670.2:g.43197620T>C	GRCh38
NC_000008.10:g.43052763T>C , CM000670.1:g.43052763T>C	GRCh37
NC_000008.9:g.43171920T>C	NCBI36
NG_009552.1:g.62172T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1543-52T>C MANE Select	ENSP00000368965.4:n.1543-52T>C
ENST00000379644.8:c.1543-52T>C	ENSP00000368965.4:n.1543-52T>C
ENST00000519705.1:n.859-52T>C
ENST00000521576.1:c.694-52T>C	ENSP00000429029.1:n.694-52T>C
ENST00000523989.1:n.1804T>C
NM_152419.2:c.1543-52T>C	NP_689632.2:n.1543-52T>C
XM_005273409.1:c.1654-52T>C	XP_005273466.1:n.1654-52T>C
XM_005273410.1:c.1630-52T>C	XP_005273467.1:n.1630-52T>C
XM_005273411.1:c.1462-52T>C	XP_005273468.1:n.1462-52T>C
NM_001363227.1:c.1630-52T>C	NP_001350156.1:n.1630-52T>C
NM_001363228.1:c.1351-52T>C	NP_001350157.1:n.1351-52T>C
NM_001363229.1:c.679-52T>C	NP_001350158.1:n.679-52T>C
NM_152419.3:c.1543-52T>C MANE Select	NP_689632.2:n.1543-52T>C
NM_001363227.2:c.1630-52T>C	NP_001350156.1:n.1630-52T>C
NM_001363228.2:c.1351-52T>C	NP_001350157.1:n.1351-52T>C
NM_001363229.2:c.679-52T>C	NP_001350158.1:n.679-52T>C