Canonical Allele Identifier: CA6747034

Gene: GNPTAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101830673C>G , CM000674.2:g.101830673C>G	GRCh38
NC_000012.11:g.102224451C>G , CM000674.1:g.102224451C>G	GRCh37
NC_000012.10:g.100748582C>G	NCBI36
NG_021243.1:g.5195G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024312.5:c.3G>C MANE Select	NP_077288.2:p.Met1Ile
ENST00000299314.12:c.3G>C MANE Select	ENSP00000299314.7:p.Met1Ile
NM_024312.4:c.3G>C	NP_077288.2:p.Met1Ile
ENST00000299314.11:c.3G>C	ENSP00000299314.7:p.Met1Ile
ENST00000392919.4:c.3G>C	ENSP00000376651.4:p.Met1Ile
ENST00000549165.1:c.3G>C	ENSP00000450413.1:p.Met1Ile
ENST00000549940.5:c.3G>C	ENSP00000449150.1:p.Met1Ile
XM_006719593.2:c.3G>C	XP_006719656.1:p.Met1Ile
XM_006719593.3:c.3G>C	XP_006719656.1:p.Met1Ile
XM_017019961.1:c.-147G>C	XP_016875450.1:n.-147G>C
XM_017019962.2:c.-1348G>C	XP_016875451.1:n.-1348G>C