Canonical Allele Identifier: CA16550557
Gene: PIEZO2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10766427A>G , CM000680.2:g.10766427A>G GRCh38
NC_000018.9:g.10766425A>G , CM000680.1:g.10766425A>G GRCh37
NC_000018.8:g.10756425A>G NCBI36
NG_034005.1:g.387336T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000383408.7:c.2947-3329T>C ENSP00000372900.4:n.2947-3329T>C
ENST00000686869.1:n.3004-3329T>C
ENST00000674853.1:c.2947-3329T>C MANE Select ENSP00000501957.1:n.2947-3329T>C
ENST00000302079.10:c.2872-3329T>C ENSP00000303316.6:n.2872-3329T>C
ENST00000383408.6:c.2723-3149T>C ENSP00000372900.3:n.2723-3149T>C
ENST00000503781.7:c.2872-3329T>C ENSP00000421377.3:n.2872-3329T>C
ENST00000580640.5:c.2947-3329T>C ENSP00000463094.1:n.2947-3329T>C
ENST00000582913.5:c.2914-3329T>C ENSP00000462115.1:n.2914-3329T>C
NM_022068.3:c.2872-3329T>C NP_071351.2:n.2872-3329T>C
XM_011525723.1:c.3004-3329T>C XP_011524025.1:n.3004-3329T>C
XM_011525724.1:c.2947-3329T>C XP_011524026.1:n.2947-3329T>C
XM_011525725.1:c.2914-3329T>C XP_011524027.1:n.2914-3329T>C
XM_011525726.1:c.3004-3329T>C XP_011524028.1:n.3004-3329T>C
XM_011525727.1:c.3004-3329T>C XP_011524029.1:n.3004-3329T>C
XM_011525723.3:c.3004-3329T>C XP_011524025.1:n.3004-3329T>C
XM_011525724.3:c.2947-3329T>C XP_011524026.1:n.2947-3329T>C
XM_011525725.3:c.2914-3329T>C XP_011524027.1:n.2914-3329T>C
XM_011525726.3:c.3004-3329T>C XP_011524028.1:n.3004-3329T>C
XM_017025918.2:c.2965-3329T>C XP_016881407.1:n.2965-3329T>C
XR_001753259.2:n.4001-3329T>C
NM_001378183.1:c.2947-3329T>C MANE Select NP_001365112.1:n.2947-3329T>C
NM_022068.4:c.2872-3329T>C NP_071351.2:n.2872-3329T>C
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