Canonical Allele Identifier: CA397101970

Gene: GALNS TRAPPC2L

Linked Data

• MyVariant Identifiers: chr16:g.88923236A>C (hg19) ; chr16:g.88856828A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88856828A>C , CM000678.2:g.88856828A>C	GRCh38
NC_000016.9:g.88923236A>C , CM000678.1:g.88923236A>C	GRCh37
NC_000016.8:g.87450737A>C	NCBI36
NG_008667.1:g.5139T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.50T>G (GALNS) MANE Select	ENSP00000268695.5:p.Leu17Arg
ENST00000268695.9:c.50T>G (GALNS)	ENSP00000268695.5:p.Leu17Arg
ENST00000564365.5:c.-398+582A>C (TRAPPC2L)	ENSP00000455447.1:n.-398+582A>C
ENST00000565364.1:n.15T>G (GALNS)
ENST00000568311.1:c.50T>G (GALNS)	ENSP00000455006.1:p.Leu17Arg
ENST00000569433.1:c.50T>G (GALNS)	ENSP00000456884.1:p.Leu17Arg
NM_000512.4:c.50T>G (GALNS)	NP_000503.1:p.Leu17Arg
XM_005256301.2:c.50T>G (GALNS)	XP_005256358.1:p.Leu17Arg
XM_005256302.1:c.-103T>G (GALNS)	XP_005256359.1:n.-103T>G
XM_011522982.1:c.-103T>G (GALNS)	XP_011521284.1:n.-103T>G
XM_011522984.1:c.-103T>G (GALNS)	XP_011521286.1:n.-103T>G
NM_001323543.1:c.-382T>G (GALNS)	NP_001310472.1:n.-382T>G
NM_001323544.1:c.-103T>G (GALNS)	NP_001310473.1:n.-103T>G
NR_134671.1:n.27+582A>C (TRAPPC2L)
XM_005256301.3:c.50T>G (GALNS)	XP_005256358.1:p.Leu17Arg
XM_011522982.2:c.-103T>G (GALNS)	XP_011521284.1:n.-103T>G
XM_017023113.1:c.-382T>G (GALNS)	XP_016878602.1:n.-382T>G
NM_000512.5:c.50T>G (GALNS) MANE Select	NP_000503.1:p.Leu17Arg
NM_001323543.2:c.-382T>G (GALNS)	NP_001310472.1:n.-382T>G
NM_001323544.2:c.-103T>G (GALNS)	NP_001310473.1:n.-103T>G
NR_134671.2:n.27+582A>C (TRAPPC2L)