Canonical Allele Identifier: CA386296307

Gene: GNPTAB

Linked Data

• MyVariant Identifiers: chr12:g.102155447T>G (hg19) ; chr12:g.101761669T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101761669T>G , CM000674.2:g.101761669T>G	GRCh38
NC_000012.11:g.102155447T>G , CM000674.1:g.102155447T>G	GRCh37
NC_000012.10:g.100679578T>G	NCBI36
NG_021243.1:g.74199A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299314.12:c.2810A>C MANE Select	ENSP00000299314.7:p.Tyr937Ser
ENST00000299314.11:c.2810A>C	ENSP00000299314.7:p.Tyr937Ser
NM_024312.4:c.2810A>C	NP_077288.2:p.Tyr937Ser
XM_006719593.2:c.2810A>C	XP_006719656.1:p.Tyr937Ser
XM_011538731.1:c.2729A>C	XP_011537033.1:p.Tyr910Ser
XM_006719593.3:c.2810A>C	XP_006719656.1:p.Tyr937Ser
XM_011538731.2:c.2729A>C	XP_011537033.1:p.Tyr910Ser
XM_017019961.1:c.2594A>C	XP_016875450.1:p.Tyr865Ser
XM_017019962.2:c.1583A>C	XP_016875451.1:p.Tyr528Ser
NM_024312.5:c.2810A>C MANE Select	NP_077288.2:p.Tyr937Ser