Canonical Allele Identifier: CA2620427177

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101757171-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101757171G>A , CM000674.2:g.101757171G>A	GRCh38
NC_000012.11:g.102150949G>A , CM000674.1:g.102150949G>A	GRCh37
NC_000012.10:g.100675080G>A	NCBI36
NG_021243.1:g.78697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.3434+41C>T MANE Select	ENSP00000299314.7:n.3434+41C>T
ENST00000299314.11:c.3434+41C>T	ENSP00000299314.7:n.3434+41C>T
ENST00000549194.1:n.341C>T
ENST00000549738.5:c.185+41C>T	ENSP00000450161.1:n.185+41C>T
ENST00000550718.1:c.246+41C>T
NM_024312.4:c.3434+41C>T	NP_077288.2:n.3434+41C>T
XM_006719593.2:c.3434+41C>T	XP_006719656.1:n.3434+41C>T
XM_011538731.1:c.3353+41C>T	XP_011537033.1:n.3353+41C>T
XM_006719593.3:c.3434+41C>T	XP_006719656.1:n.3434+41C>T
XM_011538731.2:c.3353+41C>T	XP_011537033.1:n.3353+41C>T
XM_017019961.1:c.3218+41C>T	XP_016875450.1:n.3218+41C>T
XM_017019962.2:c.2207+41C>T	XP_016875451.1:n.2207+41C>T
NM_024312.5:c.3434+41C>T MANE Select	NP_077288.2:n.3434+41C>T