Canonical Allele Identifier: CA2687149786
Gene: HGSNAT HGNC NCBI

Linked Data

gnomAD v4: 8-43140568-CCCCGGCGGCTCTTCGGGGCGCGATGCCCAGGCCGCGCCGCCACGAGGTGAGTGCACACCTCCTACCGCCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43140575_43140644del , CM000670.2:g.43140575_43140644del GRCh38
NC_000008.10:g.42995718_42995787del , CM000670.1:g.42995718_42995787del GRCh37
NC_000008.9:g.43114875_43114944del NCBI36
NG_009552.1:g.5127_5196del

Transcript Alleles

HGVS Amino-acid change
ENST00000379644.9:c.79_118+30del
ENST00000379644.8:c.79_118+30del
ENST00000517319.1:c.79_118+30del
ENST00000520704.1:c.-72_-33+30del
NM_152419.2:c.79_118+30del
XM_005273409.1:c.79_118+30del
XM_005273410.1:c.79_118+30del
XM_005273411.1:c.79_118+30del
XM_005273412.2:c.79_118+30del
NM_001363227.1:c.79_118+30del
NM_001363228.1:c.79_118+30del
NM_001363229.1:c.-755_-716+30del
XM_005273412.4:c.79_118+30del
NM_152419.3:c.79_118+30del
NM_001363227.2:c.79_118+30del
NM_001363228.2:c.79_118+30del
NM_001363229.2:c.-755_-716+30del
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