Canonical Allele Identifier: CA2671937169

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686154-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686154T>C , CM000666.2:g.121686154T>C	GRCh38
NC_000004.11:g.122607309T>C , CM000666.1:g.122607309T>C	GRCh37
NC_000004.10:g.122826759T>C	NCBI36
NG_032042.1:g.15839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+134A>G MANE Select	ENSP00000296511.5:n.94+134A>G
ENST00000296511.9:c.94+134A>G	ENSP00000296511.5:n.94+134A>G
ENST00000501272.6:c.10-2677A>G	ENSP00000424106.1:n.10-2677A>G
ENST00000506395.5:c.94+134A>G	ENSP00000421421.1:n.94+134A>G
ENST00000509016.5:n.215+134A>G
ENST00000511552.5:n.480+134A>G
ENST00000513428.5:n.259+134A>G
ENST00000513523.1:n.262+134A>G
ENST00000513728.1:c.94+134A>G	ENSP00000427135.1:n.94+134A>G
ENST00000515017.5:c.94+134A>G	ENSP00000424199.1:n.94+134A>G
NM_001154.3:c.94+134A>G	NP_001145.1:n.94+134A>G
XM_017008141.2:c.94+134A>G	XP_016863630.1:n.94+134A>G
NM_001154.4:c.94+134A>G MANE Select	NP_001145.1:n.94+134A>G