Canonical Allele Identifier: CA690978323

Gene: GAPDH

Linked Data

• dbSNP Id: rs1314881529
• MyVariant Identifiers: chr12:g.6643617_6643618insGTCCGA (hg19) ; chr12:g.6534451_6534452insGTCCGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534455_6534460dup , CM000674.2:g.6534455_6534460dup	GRCh38
NC_000012.11:g.6643621_6643626dup , CM000674.1:g.6643621_6643626dup	GRCh37
NC_000012.10:g.6513882_6513887dup	NCBI36
NG_007073.2:g.4965_4970dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.9:c.-138_-133dup	ENSP00000229239.5:n.-138_-133dup
NM_001289745.1:c.-230_-225dup	NP_001276674.1:n.-230_-225dup
NM_002046.5:c.-138_-133dup	NP_002037.2:n.-138_-133dup