Canonical Allele Identifier: CA2620448882

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101830432-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830432C>A , CM000674.2:g.101830432C>A	GRCh38
NC_000012.11:g.102224210C>A , CM000674.1:g.102224210C>A	GRCh37
NC_000012.10:g.100748341C>A	NCBI36
NG_021243.1:g.5436G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.117+127G>T MANE Select	ENSP00000299314.7:n.117+127G>T
ENST00000647144.1:n.105+127G>T
ENST00000299314.11:c.117+127G>T	ENSP00000299314.7:n.117+127G>T
ENST00000392919.4:c.117+127G>T	ENSP00000376651.4:n.117+127G>T
ENST00000549165.1:c.117+127G>T	ENSP00000450413.1:n.117+127G>T
ENST00000549940.5:c.117+127G>T	ENSP00000449150.1:n.117+127G>T
NM_024312.4:c.117+127G>T	NP_077288.2:n.117+127G>T
XM_006719593.2:c.117+127G>T	XP_006719656.1:n.117+127G>T
XM_006719593.3:c.117+127G>T	XP_006719656.1:n.117+127G>T
XM_017019961.1:c.-100+194G>T	XP_016875450.1:n.-100+194G>T
XM_017019962.2:c.-1234+127G>T	XP_016875451.1:n.-1234+127G>T
NM_024312.5:c.117+127G>T MANE Select	NP_077288.2:n.117+127G>T