Canonical Allele Identifier: CA1489952038

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686027_121686029delinsTGC , CM000666.2:g.121686027_121686029delinsTGC	GRCh38
NC_000004.11:g.122607182_122607184delinsTGC , CM000666.1:g.122607182_122607184delinsTGC	GRCh37
NC_000004.10:g.122826632_122826634delinsTGC	NCBI36
NG_032042.1:g.15964_15966delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+259_94+261delinsGCA MANE Select	ENSP00000296511.5:n.94+259_94+261delinsGCA
ENST00000296511.9:c.94+259_94+261delinsGCA	ENSP00000296511.5:n.94+259_94+261delinsGCA
ENST00000501272.6:c.10-2552_10-2550delinsGCA	ENSP00000424106.1:n.10-2552_10-2550delinsGCA
ENST00000506395.5:c.94+259_94+261delinsGCA	ENSP00000421421.1:n.94+259_94+261delinsGCA
ENST00000509016.5:n.215+259_215+261delinsGCA
ENST00000511552.5:n.480+259_480+261delinsGCA
ENST00000513428.5:n.259+259_259+261delinsGCA
ENST00000513523.1:n.262+259_262+261delinsGCA
ENST00000513728.1:c.94+259_94+261delinsGCA	ENSP00000427135.1:n.94+259_94+261delinsGCA
ENST00000515017.5:c.94+259_94+261delinsGCA	ENSP00000424199.1:n.94+259_94+261delinsGCA
NM_001154.3:c.94+259_94+261delinsGCA	NP_001145.1:n.94+259_94+261delinsGCA
XM_017008141.2:c.94+259_94+261delinsGCA	XP_016863630.1:n.94+259_94+261delinsGCA
NM_001154.4:c.94+259_94+261delinsGCA MANE Select	NP_001145.1:n.94+259_94+261delinsGCA