Canonical Allele Identifier: CA2797216498

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830766T>G , CM000674.2:g.101830766T>G	GRCh38
NC_000012.11:g.102224544T>G , CM000674.1:g.102224544T>G	GRCh37
NC_000012.10:g.100748675T>G	NCBI36
NG_021243.1:g.5102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.-91A>C MANE Select	ENSP00000299314.7:n.-91A>C
ENST00000299314.11:c.-91A>C	ENSP00000299314.7:n.-91A>C
ENST00000392919.4:c.-91A>C	ENSP00000376651.4:n.-91A>C
ENST00000549940.5:c.-91A>C	ENSP00000449150.1:n.-91A>C
NM_024312.4:c.-91A>C	NP_077288.2:n.-91A>C
XM_006719593.2:c.-91A>C	XP_006719656.1:n.-91A>C
XM_006719593.3:c.-91A>C	XP_006719656.1:n.-91A>C
XM_017019961.1:c.-240A>C	XP_016875450.1:n.-240A>C
XM_017019962.2:c.-1441A>C	XP_016875451.1:n.-1441A>C
NM_024312.5:c.-91A>C MANE Select	NP_077288.2:n.-91A>C