Canonical Allele Identifier: CA1489951928

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685812_121685813delinsTC , CM000666.2:g.121685812_121685813delinsTC	GRCh38
NC_000004.11:g.122606967_122606968delinsTC , CM000666.1:g.122606967_122606968delinsTC	GRCh37
NC_000004.10:g.122826417_122826418delinsTC	NCBI36
NG_032042.1:g.16180_16181delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+475_94+476delinsGA MANE Select	ENSP00000296511.5:n.94+475_94+476delinsGA
ENST00000296511.9:c.94+475_94+476delinsGA	ENSP00000296511.5:n.94+475_94+476delinsGA
ENST00000501272.6:c.10-2336_10-2335delinsGA	ENSP00000424106.1:n.10-2336_10-2335delinsGA
ENST00000506395.5:c.94+475_94+476delinsGA	ENSP00000421421.1:n.94+475_94+476delinsGA
ENST00000509016.5:n.215+475_215+476delinsGA
ENST00000511552.5:n.480+475_480+476delinsGA
ENST00000513428.5:n.259+475_259+476delinsGA
ENST00000513523.1:n.262+475_262+476delinsGA
ENST00000513728.1:c.94+475_94+476delinsGA	ENSP00000427135.1:n.94+475_94+476delinsGA
ENST00000515017.5:c.94+475_94+476delinsGA	ENSP00000424199.1:n.94+475_94+476delinsGA
NM_001154.3:c.94+475_94+476delinsGA	NP_001145.1:n.94+475_94+476delinsGA
XM_017008141.2:c.94+475_94+476delinsGA	XP_016863630.1:n.94+475_94+476delinsGA
NM_001154.4:c.94+475_94+476delinsGA MANE Select	NP_001145.1:n.94+475_94+476delinsGA