Canonical Allele Identifier: CA2671937994

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696878-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696878C>A , CM000666.2:g.121696878C>A	GRCh38
NC_000004.11:g.122618033C>A , CM000666.1:g.122618033C>A	GRCh37
NC_000004.10:g.122837483C>A	NCBI36
NG_032042.1:g.5115G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-51G>T MANE Select	ENSP00000296511.5:n.-51G>T
ENST00000296511.9:c.-51G>T	ENSP00000296511.5:n.-51G>T
ENST00000501272.6:c.-51G>T	ENSP00000424106.1:n.-51G>T
ENST00000506395.5:c.-51G>T	ENSP00000421421.1:n.-51G>T
ENST00000509016.5:n.115G>T
ENST00000511552.5:n.98G>T
ENST00000513428.5:n.115G>T
ENST00000513523.1:n.118G>T
ENST00000513728.1:c.-51G>T	ENSP00000427135.1:n.-51G>T
ENST00000515017.5:c.-51G>T	ENSP00000424199.1:n.-51G>T
NM_001154.3:c.-51G>T	NP_001145.1:n.-51G>T
XM_017008141.2:c.-51G>T	XP_016863630.1:n.-51G>T
NM_001154.4:c.-51G>T MANE Select	NP_001145.1:n.-51G>T