Canonical Allele Identifier: CA2634890601

Gene: GALNS

Linked Data

• gnomAD v4: 16-88826582-A-AGGGCCATCAATGGCCCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88826582_88826583insGGGCCATCAATGGCCCTGT , CM000678.2:g.88826582_88826583insGGGCCATCAATGGCCCTGT	GRCh38
NC_000016.9:g.88892990_88892991insGGGCCATCAATGGCCCTGT , CM000678.1:g.88892990_88892991insGGGCCATCAATGGCCCTGT	GRCh37
NC_000016.8:g.87420491_87420492insGGGCCATCAATGGCCCTGT	NCBI36
NG_008667.1:g.35384_35385insACAGGGCCATTGATGGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.1139+119_1139+120insACAGGGCCATTGATGGCCC MANE Select	ENSP00000268695.5:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
ENST00000268695.9:c.1139+119_1139+120insACAGGGCCATTGATGGCCC	ENSP00000268695.5:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
ENST00000562593.5:n.4548+119_4548+120insACAGGGCCATTGATGGCCC
ENST00000564263.1:n.415+119_415+120insACAGGGCCATTGATGGCCC
ENST00000567525.5:c.820+119_820+120insACAGGGCCATTGATGGCCC	ENSP00000454484.1:n.820+119_820+120insACAGGGCCATTGATGGCCC
ENST00000568613.5:c.1258+119_1258+120insACAGGGCCATTGATGGCCC	ENSP00000457921.1:n.1258+119_1258+120insACAGGGCCATTGATGGCCC
NM_000512.4:c.1139+119_1139+120insACAGGGCCATTGATGGCCC	NP_000503.1:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
XM_005256301.2:c.1139+119_1139+120insACAGGGCCATTGATGGCCC	XP_005256358.1:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
XM_005256302.1:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_005256359.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_011522982.1:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_011521284.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_011522984.1:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_011521286.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
NM_001323543.1:c.584+119_584+120insACAGGGCCATTGATGGCCC	NP_001310472.1:n.584+119_584+120insACAGGGCCATTGATGGCCC
NM_001323544.1:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	NP_001310473.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_005256301.3:c.1139+119_1139+120insACAGGGCCATTGATGGCCC	XP_005256358.1:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
XM_011522982.2:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_011521284.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_017023111.2:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_016878600.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_017023112.2:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	XP_016878601.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC
XM_017023113.1:c.584+119_584+120insACAGGGCCATTGATGGCCC	XP_016878602.1:n.584+119_584+120insACAGGGCCATTGATGGCCC
NM_000512.5:c.1139+119_1139+120insACAGGGCCATTGATGGCCC MANE Select	NP_000503.1:n.1139+119_1139+120insACAGGGCCATTGATGGCCC
NM_001323543.2:c.584+119_584+120insACAGGGCCATTGATGGCCC	NP_001310472.1:n.584+119_584+120insACAGGGCCATTGATGGCCC
NM_001323544.2:c.1157+119_1157+120insACAGGGCCATTGATGGCCC	NP_001310473.1:n.1157+119_1157+120insACAGGGCCATTGATGGCCC