Canonical Allele Identifier: CA2671937900

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696818-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696822_121696824del , CM000666.2:g.121696822_121696824del	GRCh38
NC_000004.11:g.122617977_122617979del , CM000666.1:g.122617977_122617979del	GRCh37
NC_000004.10:g.122837427_122837429del	NCBI36
NG_032042.1:g.5172_5174del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-36+42_-36+44del MANE Select	ENSP00000296511.5:n.-36+42_-36+44del
ENST00000296511.9:c.-36+42_-36+44del	ENSP00000296511.5:n.-36+42_-36+44del
ENST00000501272.6:c.-36+42_-36+44del	ENSP00000424106.1:n.-36+42_-36+44del
ENST00000506395.5:c.-36+42_-36+44del	ENSP00000421421.1:n.-36+42_-36+44del
ENST00000509016.5:n.130+42_130+44del
ENST00000511552.5:n.155_157del
ENST00000513428.5:n.130+42_130+44del
ENST00000513523.1:n.133+42_133+44del
ENST00000513728.1:c.-36+42_-36+44del	ENSP00000427135.1:n.-36+42_-36+44del
ENST00000515017.5:c.-36+42_-36+44del	ENSP00000424199.1:n.-36+42_-36+44del
NM_001154.3:c.-36+42_-36+44del	NP_001145.1:n.-36+42_-36+44del
XM_017008141.2:c.-36+42_-36+44del	XP_016863630.1:n.-36+42_-36+44del
NM_001154.4:c.-36+42_-36+44del MANE Select	NP_001145.1:n.-36+42_-36+44del