Canonical Allele Identifier: CA386296185

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155390T>G (hg19) ; chr12:g.101761612T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761612T>G , CM000674.2:g.101761612T>G	GRCh38
NC_000012.11:g.102155390T>G , CM000674.1:g.102155390T>G	GRCh37
NC_000012.10:g.100679521T>G	NCBI36
NG_021243.1:g.74256A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2867A>C MANE Select	ENSP00000299314.7:p.His956Pro
ENST00000299314.11:c.2867A>C	ENSP00000299314.7:p.His956Pro
NM_024312.4:c.2867A>C	NP_077288.2:p.His956Pro
XM_006719593.2:c.2867A>C	XP_006719656.1:p.His956Pro
XM_011538731.1:c.2786A>C	XP_011537033.1:p.His929Pro
XM_006719593.3:c.2867A>C	XP_006719656.1:p.His956Pro
XM_011538731.2:c.2786A>C	XP_011537033.1:p.His929Pro
XM_017019961.1:c.2651A>C	XP_016875450.1:p.His884Pro
XM_017019962.2:c.1640A>C	XP_016875451.1:p.His547Pro
NM_024312.5:c.2867A>C MANE Select	NP_077288.2:p.His956Pro