Canonical Allele Identifier: CA359192164

Gene: DNAH5

Linked Data

• COSMIC: COSM3850392
• MyVariant Identifiers: chr5:g.13753603C>A (hg19) ; chr5:g.13753494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753494C>A , CM000667.2:g.13753494C>A	GRCh38
NC_000005.9:g.13753603C>A , CM000667.1:g.13753603C>A	GRCh37
NC_000005.8:g.13806603C>A	NCBI36
NG_013081.1:g.195987G>T
NG_013081.2:g.195987G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10611G>T MANE Select	ENSP00000265104.4:p.Glu3537Asp
ENST00000681290.1:c.10566G>T	ENSP00000505288.1:p.Glu3522Asp
ENST00000265104.4:c.10611G>T	ENSP00000265104.4:p.Glu3537Asp
NM_001369.2:c.10611G>T	NP_001360.1:p.Glu3537Asp
XM_005248262.2:c.10566G>T	XP_005248319.1:p.Glu3522Asp
XM_005248262.3:c.10719G>T	XP_005248319.2:p.Glu3573Asp
XM_017009177.1:c.10719G>T	XP_016864666.1:p.Glu3573Asp
XM_017009178.1:c.9624G>T	XP_016864667.1:p.Glu3208Asp
XM_017009179.2:c.9624G>T	XP_016864668.1:p.Glu3208Asp
XM_017009180.1:c.10719G>T	XP_016864669.1:p.Glu3573Asp
XM_017009181.1:c.10719G>T	XP_016864670.1:p.Glu3573Asp
XM_017009182.1:c.10719G>T	XP_016864671.1:p.Glu3573Asp
XM_017009185.1:c.5808G>T	XP_016864674.1:p.Glu1936Asp
XM_017009186.1:c.5361G>T	XP_016864675.1:p.Glu1787Asp
XM_017009188.1:c.4698G>T	XP_016864677.1:p.Glu1566Asp
XM_024454388.1:c.9624G>T	XP_024310156.1:p.Glu3208Asp
XM_024454389.1:c.9213G>T	XP_024310157.1:p.Glu3071Asp
NM_001369.3:c.10611G>T MANE Select	NP_001360.1:p.Glu3537Asp