Canonical Allele Identifier: CA359189759

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13752272T>A (hg19) ; chr5:g.13752163T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752163T>A , CM000667.2:g.13752163T>A	GRCh38
NC_000005.9:g.13752272T>A , CM000667.1:g.13752272T>A	GRCh37
NC_000005.8:g.13805272T>A	NCBI36
NG_013081.1:g.197318A>T
NG_013081.2:g.197318A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10999A>T MANE Select	ENSP00000265104.4:p.Asn3667Tyr
ENST00000681290.1:c.10954A>T	ENSP00000505288.1:p.Asn3652Tyr
ENST00000265104.4:c.10999A>T	ENSP00000265104.4:p.Asn3667Tyr
NM_001369.2:c.10999A>T	NP_001360.1:p.Asn3667Tyr
XM_005248262.2:c.10954A>T	XP_005248319.1:p.Asn3652Tyr
XM_005248262.3:c.11107A>T	XP_005248319.2:p.Asn3703Tyr
XM_017009177.1:c.11107A>T	XP_016864666.1:p.Asn3703Tyr
XM_017009178.1:c.10012A>T	XP_016864667.1:p.Asn3338Tyr
XM_017009179.2:c.10012A>T	XP_016864668.1:p.Asn3338Tyr
XM_017009180.1:c.11107A>T	XP_016864669.1:p.Asn3703Tyr
XM_017009181.1:c.11107A>T	XP_016864670.1:p.Asn3703Tyr
XM_017009182.1:c.11107A>T	XP_016864671.1:p.Asn3703Tyr
XM_017009185.1:c.6196A>T	XP_016864674.1:p.Asn2066Tyr
XM_017009186.1:c.5749A>T	XP_016864675.1:p.Asn1917Tyr
XM_017009188.1:c.5086A>T	XP_016864677.1:p.Asn1696Tyr
XM_024454388.1:c.10012A>T	XP_024310156.1:p.Asn3338Tyr
XM_024454389.1:c.9601A>T	XP_024310157.1:p.Asn3201Tyr
NM_001369.3:c.10999A>T MANE Select	NP_001360.1:p.Asn3667Tyr