Canonical Allele Identifier: CA386303413

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101770995C>A , CM000674.2:g.101770995C>A	GRCh38
NC_000012.11:g.102164773C>A , CM000674.1:g.102164773C>A	GRCh37
NC_000012.10:g.100688904C>A	NCBI36
NG_021243.1:g.64873G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024312.5:c.933+1G>T MANE Select	NP_077288.2:n.933+1G>T
ENST00000299314.12:c.933+1G>T MANE Select	ENSP00000299314.7:n.933+1G>T
NM_024312.4:c.933+1G>T	NP_077288.2:n.933+1G>T
ENST00000299314.11:c.933+1G>T	ENSP00000299314.7:n.933+1G>T
ENST00000549940.5:c.933+1G>T	ENSP00000449150.1:n.933+1G>T
XM_006719593.2:c.933+1G>T	XP_006719656.1:n.933+1G>T
XM_006719593.3:c.933+1G>T	XP_006719656.1:n.933+1G>T
XM_011538731.1:c.852+1G>T	XP_011537033.1:n.852+1G>T
XM_011538731.2:c.852+1G>T	XP_011537033.1:n.852+1G>T
XM_017019961.1:c.717+1G>T	XP_016875450.1:n.717+1G>T
XM_017019962.2:c.-418+1G>T	XP_016875451.1:n.-418+1G>T