Canonical Allele Identifier: CA2671937969

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696863-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696863C>T , CM000666.2:g.121696863C>T	GRCh38
NC_000004.11:g.122618018C>T , CM000666.1:g.122618018C>T	GRCh37
NC_000004.10:g.122837468C>T	NCBI36
NG_032042.1:g.5130G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-36G>A MANE Select	ENSP00000296511.5:n.-36G>A
ENST00000296511.9:c.-36G>A	ENSP00000296511.5:n.-36G>A
ENST00000501272.6:c.-36G>A	ENSP00000424106.1:n.-36G>A
ENST00000506395.5:c.-36G>A	ENSP00000421421.1:n.-36G>A
ENST00000509016.5:n.130G>A
ENST00000511552.5:n.113G>A
ENST00000513428.5:n.130G>A
ENST00000513523.1:n.133G>A
ENST00000513728.1:c.-36G>A	ENSP00000427135.1:n.-36G>A
ENST00000515017.5:c.-36G>A	ENSP00000424199.1:n.-36G>A
NM_001154.3:c.-36G>A	NP_001145.1:n.-36G>A
XM_017008141.2:c.-36G>A	XP_016863630.1:n.-36G>A
NM_001154.4:c.-36G>A MANE Select	NP_001145.1:n.-36G>A