Canonical Allele Identifier: CA386486872

Gene: GNPTAB

Linked Data

• gnomAD v4: 12-101830563-C-G
• MyVariant Identifiers: chr12:g.102224341C>G (hg19) ; chr12:g.101830563C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830563C>G , CM000674.2:g.101830563C>G	GRCh38
NC_000012.11:g.102224341C>G , CM000674.1:g.102224341C>G	GRCh37
NC_000012.10:g.100748472C>G	NCBI36
NG_021243.1:g.5305G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299314.12:c.113G>C MANE Select	ENSP00000299314.7:p.Gly38Ala
ENST00000647144.1:n.101G>C
ENST00000299314.11:c.113G>C	ENSP00000299314.7:p.Gly38Ala
ENST00000392919.4:c.113G>C	ENSP00000376651.4:p.Gly38Ala
ENST00000549165.1:c.113G>C	ENSP00000450413.1:p.Gly38Ala
ENST00000549940.5:c.113G>C	ENSP00000449150.1:p.Gly38Ala
NM_024312.4:c.113G>C	NP_077288.2:p.Gly38Ala
XM_006719593.2:c.113G>C	XP_006719656.1:p.Gly38Ala
XM_006719593.3:c.113G>C	XP_006719656.1:p.Gly38Ala
XM_017019961.1:c.-100+63G>C	XP_016875450.1:n.-100+63G>C
XM_017019962.2:c.-1238G>C	XP_016875451.1:n.-1238G>C
NM_024312.5:c.113G>C MANE Select	NP_077288.2:p.Gly38Ala