Canonical Allele Identifier: CA2740934642

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192090G>T , CM000670.2:g.43192090G>T	GRCh38
NC_000008.10:g.43047233G>T , CM000670.1:g.43047233G>T	GRCh37
NC_000008.9:g.43166390G>T	NCBI36
NG_009552.1:g.56642G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1251-214G>T MANE Select	ENSP00000368965.4:n.1251-214G>T
ENST00000379644.8:c.1251-214G>T	ENSP00000368965.4:n.1251-214G>T
ENST00000520678.1:n.184-214G>T
ENST00000521576.1:c.402-214G>T	ENSP00000429029.1:n.402-214G>T
ENST00000524016.5:c.355-214G>T
NM_152419.2:c.1251-214G>T	NP_689632.2:n.1251-214G>T
XM_005273409.1:c.1251-214G>T	XP_005273466.1:n.1251-214G>T
XM_005273410.1:c.1251-214G>T	XP_005273467.1:n.1251-214G>T
XM_005273411.1:c.1059-214G>T	XP_005273468.1:n.1059-214G>T
XM_005273412.2:c.1251-214G>T	XP_005273469.1:n.1251-214G>T
NM_001363227.1:c.1251-214G>T	NP_001350156.1:n.1251-214G>T
NM_001363228.1:c.1059-214G>T	NP_001350157.1:n.1059-214G>T
NM_001363229.1:c.387-214G>T	NP_001350158.1:n.387-214G>T
XM_005273412.4:c.1251-214G>T	XP_005273469.1:n.1251-214G>T
NM_152419.3:c.1251-214G>T MANE Select	NP_689632.2:n.1251-214G>T
NM_001363227.2:c.1251-214G>T	NP_001350156.1:n.1251-214G>T
NM_001363228.2:c.1059-214G>T	NP_001350157.1:n.1059-214G>T
NM_001363229.2:c.387-214G>T	NP_001350158.1:n.387-214G>T