Canonical Allele Identifier: CA554174437

Gene: ANXA5

Linked Data

• gnomAD v2: 4-122607213-TCA-T
• gnomAD v3: 4-121686058-TCA-T
• gnomAD v4: 4-121686058-TCA-T
• MyVariant Identifiers: chr4:g.122607214_122607215del (hg19) ; chr4:g.121686059_121686060del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686059_121686060del , CM000666.2:g.121686059_121686060del	GRCh38
NC_000004.11:g.122607214_122607215del , CM000666.1:g.122607214_122607215del	GRCh37
NC_000004.10:g.122826664_122826665del	NCBI36
NG_032042.1:g.15933_15934del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+228_94+229del MANE Select	ENSP00000296511.5:n.94+228_94+229del
ENST00000296511.9:c.94+228_94+229del	ENSP00000296511.5:n.94+228_94+229del
ENST00000501272.6:c.10-2583_10-2582del	ENSP00000424106.1:n.10-2583_10-2582del
ENST00000506395.5:c.94+228_94+229del	ENSP00000421421.1:n.94+228_94+229del
ENST00000509016.5:n.215+228_215+229del
ENST00000511552.5:n.480+228_480+229del
ENST00000513428.5:n.259+228_259+229del
ENST00000513523.1:n.262+228_262+229del
ENST00000513728.1:c.94+228_94+229del	ENSP00000427135.1:n.94+228_94+229del
ENST00000515017.5:c.94+228_94+229del	ENSP00000424199.1:n.94+228_94+229del
NM_001154.3:c.94+228_94+229del	NP_001145.1:n.94+228_94+229del
XM_017008141.2:c.94+228_94+229del	XP_016863630.1:n.94+228_94+229del
NM_001154.4:c.94+228_94+229del MANE Select	NP_001145.1:n.94+228_94+229del