Canonical Allele Identifier: CA5923419
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22270406_22270409dup , CM000673.2:g.22270406_22270409dup GRCh38
NC_000011.9:g.22291952_22291955dup , CM000673.1:g.22291952_22291955dup GRCh37
NC_000011.8:g.22248528_22248531dup NCBI36
NG_015844.1:g.82231_82234dup , LRG_868:g.82231_82234dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000532043.2:n.10_13dup
ENST00000682266.1:c.1543_1546dup ENSP00000507766.1:p.Pro516ArgfsTer8
ENST00000682341.1:c.1951_1954dup ENSP00000508251.1:p.Pro652ArgfsTer8
ENST00000683197.1:c.1951_1954dup ENSP00000507641.1:p.Pro652ArgfsTer8
ENST00000683411.1:c.1543_1546dup ENSP00000508397.1:p.Pro516ArgfsTer8
ENST00000683437.1:c.1543_1546dup ENSP00000508408.1:p.Pro516ArgfsTer8
ENST00000683613.1:n.2987_2990dup
ENST00000684663.1:c.1948_1951dup ENSP00000508009.1:p.Pro651ArgfsTer8
ENST00000324559.9:c.1993_1996dup MANE Select ENSP00000315371.9:p.Pro666ArgfsTer8
ENST00000648804.1:n.2328_2331dup
ENST00000324559.8:c.1993_1996dup ENSP00000315371.8:p.Pro666ArgfsTer8
ENST00000532043.1:n.10_13dup
NM_001142649.1:c.1990_1993dup NP_001136121.1:p.Pro665ArgfsTer8
NM_213599.2:c.1993_1996dup , LRG_868t1:c.1993_1996dup NP_998764.1:p.Pro666ArgfsTer8
XM_005252820.2:c.1951_1954dup XP_005252877.2:p.Pro652ArgfsTer8
XM_005252821.2:c.1948_1951dup XP_005252878.2:p.Pro651ArgfsTer8
XM_005252822.3:c.1915_1918dup XP_005252879.1:p.Pro640ArgfsTer8
XM_005252823.3:c.1912_1915dup XP_005252880.1:p.Pro639ArgfsTer8
XM_011519949.1:c.1900_1903dup XP_011518251.1:p.Pro635ArgfsTer8
XM_005252820.3:c.1951_1954dup XP_005252877.2:p.Pro652ArgfsTer8
XM_005252821.3:c.1948_1951dup XP_005252878.2:p.Pro651ArgfsTer8
XM_005252822.4:c.1915_1918dup XP_005252879.1:p.Pro640ArgfsTer8
XM_011519949.2:c.1900_1903dup XP_011518251.1:p.Pro635ArgfsTer8
NM_001142649.2:c.1990_1993dup NP_001136121.1:p.Pro665ArgfsTer8
NM_213599.3:c.1993_1996dup MANE Select NP_998764.1:p.Pro666ArgfsTer8