Canonical Allele Identifier: CA1489952237

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686420_121686421delinsCA , CM000666.2:g.121686420_121686421delinsCA	GRCh38
NC_000004.11:g.122607575_122607576delinsCA , CM000666.1:g.122607575_122607576delinsCA	GRCh37
NC_000004.10:g.122827025_122827026delinsCA	NCBI36
NG_032042.1:g.15572_15573delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-49_10-48delinsTG MANE Select	ENSP00000296511.5:n.10-49_10-48delinsTG
ENST00000296511.9:c.10-49_10-48delinsTG	ENSP00000296511.5:n.10-49_10-48delinsTG
ENST00000501272.6:c.10-2944_10-2943delinsTG	ENSP00000424106.1:n.10-2944_10-2943delinsTG
ENST00000506395.5:c.10-49_10-48delinsTG	ENSP00000421421.1:n.10-49_10-48delinsTG
ENST00000509016.5:n.131-49_131-48delinsTG
ENST00000511552.5:n.396-49_396-48delinsTG
ENST00000513428.5:n.175-49_175-48delinsTG
ENST00000513523.1:n.178-49_178-48delinsTG
ENST00000513728.1:c.10-49_10-48delinsTG	ENSP00000427135.1:n.10-49_10-48delinsTG
ENST00000515017.5:c.10-49_10-48delinsTG	ENSP00000424199.1:n.10-49_10-48delinsTG
NM_001154.3:c.10-49_10-48delinsTG	NP_001145.1:n.10-49_10-48delinsTG
XM_017008141.2:c.10-49_10-48delinsTG	XP_016863630.1:n.10-49_10-48delinsTG
NM_001154.4:c.10-49_10-48delinsTG MANE Select	NP_001145.1:n.10-49_10-48delinsTG