Canonical Allele Identifier: CA359204347
Community Standard Title: NM_001369.3(DNAH5):c.9555T>A (p.Tyr3185Ter)
Gene: DNAH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13770799A>T , CM000667.2:g.13770799A>T GRCh38
NC_000005.9:g.13770908A>T , CM000667.1:g.13770908A>T GRCh37
NC_000005.8:g.13823908A>T NCBI36
NG_013081.1:g.178682T>A
NG_013081.2:g.178682T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001369.3:c.9555T>A MANE Select NP_001360.1:p.Tyr3185Ter
ENST00000265104.5:c.9555T>A MANE Select ENSP00000265104.4:p.Tyr3185Ter
NM_001369.2:c.9555T>A NP_001360.1:p.Tyr3185Ter
ENST00000265104.4:c.9555T>A ENSP00000265104.4:p.Tyr3185Ter
ENST00000504001.3:n.267T>A
ENST00000681290.1:c.9510T>A ENSP00000505288.1:p.Tyr3170Ter
XM_005248262.2:c.9510T>A XP_005248319.1:p.Tyr3170Ter
XM_005248262.3:c.9663T>A XP_005248319.2:p.Tyr3221Ter
XM_017009177.1:c.9663T>A XP_016864666.1:p.Tyr3221Ter
XM_017009178.1:c.8568T>A XP_016864667.1:p.Tyr2856Ter
XM_017009179.2:c.8568T>A XP_016864668.1:p.Tyr2856Ter
XM_017009180.1:c.9663T>A XP_016864669.1:p.Tyr3221Ter
XM_017009181.1:c.9663T>A XP_016864670.1:p.Tyr3221Ter
XM_017009182.1:c.9663T>A XP_016864671.1:p.Tyr3221Ter
XM_017009183.1:c.9663T>A XP_016864672.1:p.Tyr3221Ter
XM_017009185.1:c.4752T>A XP_016864674.1:p.Tyr1584Ter
XM_017009186.1:c.4305T>A XP_016864675.1:p.Tyr1435Ter
XM_017009188.1:c.3642T>A XP_016864677.1:p.Tyr1214Ter
XM_024454388.1:c.8568T>A XP_024310156.1:p.Tyr2856Ter
XM_024454389.1:c.8157T>A XP_024310157.1:p.Tyr2719Ter