Canonical Allele Identifier: CA358037359

Gene: ANXA5

Linked Data

• MyVariant Identifiers: chr4:g.122607491C>A (hg19) ; chr4:g.121686336C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686336C>A , CM000666.2:g.121686336C>A	GRCh38
NC_000004.11:g.122607491C>A , CM000666.1:g.122607491C>A	GRCh37
NC_000004.10:g.122826941C>A	NCBI36
NG_032042.1:g.15657G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.46G>T MANE Select	ENSP00000296511.5:p.Asp16Tyr
ENST00000296511.9:c.46G>T	ENSP00000296511.5:p.Asp16Tyr
ENST00000501272.6:c.10-2859G>T	ENSP00000424106.1:n.10-2859G>T
ENST00000506395.5:c.46G>T	ENSP00000421421.1:p.Asp16Tyr
ENST00000509016.5:n.167G>T
ENST00000511552.5:n.432G>T
ENST00000513428.5:n.211G>T
ENST00000513523.1:n.214G>T
ENST00000513728.1:c.46G>T	ENSP00000427135.1:p.Asp16Tyr
ENST00000515017.5:c.46G>T	ENSP00000424199.1:p.Asp16Tyr
NM_001154.3:c.46G>T	NP_001145.1:p.Asp16Tyr
XM_017008141.2:c.46G>T	XP_016863630.1:p.Asp16Tyr
NM_001154.4:c.46G>T MANE Select	NP_001145.1:p.Asp16Tyr