Canonical Allele Identifier: CA397100978

Gene: GALNS TRAPPC2L

Linked Data

• gnomAD v4: 16-88856761-G-T
• MyVariant Identifiers: chr16:g.88923169G>T (hg19) ; chr16:g.88856761G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88856761G>T , CM000678.2:g.88856761G>T	GRCh38
NC_000016.9:g.88923169G>T , CM000678.1:g.88923169G>T	GRCh37
NC_000016.8:g.87450670G>T	NCBI36
NG_008667.1:g.5206C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.117C>A (GALNS) MANE Select	ENSP00000268695.5:p.Asp39Glu
ENST00000268695.9:c.117C>A (GALNS)	ENSP00000268695.5:p.Asp39Glu
ENST00000564365.5:c.-398+515G>T (TRAPPC2L)	ENSP00000455447.1:n.-398+515G>T
ENST00000565364.1:n.82C>A (GALNS)
ENST00000567525.5:c.66C>A (GALNS)	ENSP00000454484.1:p.Asp22Glu
ENST00000568311.1:c.117C>A (GALNS)	ENSP00000455006.1:p.Asp39Glu
ENST00000568613.5:c.66C>A (GALNS)	ENSP00000457921.1:p.Asp22Glu
ENST00000569433.1:c.117C>A (GALNS)	ENSP00000456884.1:p.Asp39Glu
NM_000512.4:c.117C>A (GALNS)	NP_000503.1:p.Asp39Glu
XM_005256301.2:c.117C>A (GALNS)	XP_005256358.1:p.Asp39Glu
XM_005256302.1:c.-36C>A (GALNS)	XP_005256359.1:n.-36C>A
XM_011522982.1:c.-36C>A (GALNS)	XP_011521284.1:n.-36C>A
XM_011522984.1:c.-36C>A (GALNS)	XP_011521286.1:n.-36C>A
NM_001323543.1:c.-315C>A (GALNS)	NP_001310472.1:n.-315C>A
NM_001323544.1:c.-36C>A (GALNS)	NP_001310473.1:n.-36C>A
NR_134671.1:n.27+515G>T (TRAPPC2L)
XM_005256301.3:c.117C>A (GALNS)	XP_005256358.1:p.Asp39Glu
XM_011522982.2:c.-36C>A (GALNS)	XP_011521284.1:n.-36C>A
XM_017023113.1:c.-315C>A (GALNS)	XP_016878602.1:n.-315C>A
NM_000512.5:c.117C>A (GALNS) MANE Select	NP_000503.1:p.Asp39Glu
NM_001323543.2:c.-315C>A (GALNS)	NP_001310472.1:n.-315C>A
NM_001323544.2:c.-36C>A (GALNS)	NP_001310473.1:n.-36C>A
NR_134671.2:n.27+515G>T (TRAPPC2L)