Canonical Allele Identifier: CA386304996

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101786119-G-A
• MyVariant Identifiers: chr12:g.102179897G>A (hg19) ; chr12:g.101786119G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101786119G>A , CM000674.2:g.101786119G>A	GRCh38
NC_000012.11:g.102179897G>A , CM000674.1:g.102179897G>A	GRCh37
NC_000012.10:g.100704028G>A	NCBI36
NG_021243.1:g.49749C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.464C>T MANE Select	ENSP00000299314.7:p.Pro155Leu
ENST00000299314.11:c.464C>T	ENSP00000299314.7:p.Pro155Leu
ENST00000549940.5:c.464C>T	ENSP00000449150.1:p.Pro155Leu
ENST00000550352.1:n.258C>T
ENST00000552681.1:c.98C>T	ENSP00000449217.1:p.Pro33Leu
NM_024312.4:c.464C>T	NP_077288.2:p.Pro155Leu
XM_006719593.2:c.464C>T	XP_006719656.1:p.Pro155Leu
XM_011538731.1:c.383C>T	XP_011537033.1:p.Pro128Leu
XM_006719593.3:c.464C>T	XP_006719656.1:p.Pro155Leu
XM_011538731.2:c.383C>T	XP_011537033.1:p.Pro128Leu
XM_017019961.1:c.248C>T	XP_016875450.1:p.Pro83Leu
XM_017019962.2:c.-887C>T	XP_016875451.1:n.-887C>T
NM_024312.5:c.464C>T MANE Select	NP_077288.2:p.Pro155Leu