Canonical Allele Identifier: CA1470604737
Community Standard Title: NM_005139.3(ANXA3):c.313-550G>C
Gene: ANXA3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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