Canonical Allele Identifier: CA798777804
Community Standard Title: NM_005139.3(ANXA3):c.313-550G>A
Gene: ANXA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78585710G>A , CM000666.2:g.78585710G>A GRCh38
NC_000004.11:g.79506864G>A , CM000666.1:g.79506864G>A GRCh37
NC_000004.10:g.79725888G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_005139.3:c.313-550G>A MANE Select NP_005130.1:n.313-550G>A
ENST00000264908.11:c.313-550G>A MANE Select ENSP00000264908.6:n.313-550G>A
NM_005139.2:c.313-550G>A NP_005130.1:n.313-550G>A
ENST00000264908.10:c.313-550G>A ENSP00000264908.6:n.313-550G>A
ENST00000503570.6:c.196-550G>A ENSP00000421015.2:n.196-550G>A
ENST00000508214.1:c.313-550G>A ENSP00000422281.1:n.313-550G>A
ENST00000512542.5:c.16-9671G>A ENSP00000426591.1:n.16-9671G>A
ENST00000512884.5:c.196-550G>A ENSP00000423068.1:n.196-550G>A
ENST00000514171.5:c.313-550G>A ENSP00000421512.1:n.313-550G>A
XM_011531906.1:c.370-550G>A XP_011530208.1:n.370-550G>A
XR_001741215.2:n.450-550G>A
XR_938727.1:n.472-550G>A