Canonical Allele Identifier: CA359225319

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13736036T>A (hg19) ; chr5:g.13735927T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13735927T>A , CM000667.2:g.13735927T>A	GRCh38
NC_000005.9:g.13736036T>A , CM000667.1:g.13736036T>A	GRCh37
NC_000005.8:g.13789036T>A	NCBI36
NG_013081.1:g.213554A>T
NG_013081.2:g.213554A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.11461A>T MANE Select	ENSP00000265104.4:p.Thr3821Ser
ENST00000681290.1:c.11416A>T	ENSP00000505288.1:p.Thr3806Ser
ENST00000265104.4:c.11461A>T	ENSP00000265104.4:p.Thr3821Ser
NM_001369.2:c.11461A>T	NP_001360.1:p.Thr3821Ser
XM_005248262.2:c.11416A>T	XP_005248319.1:p.Thr3806Ser
XM_005248262.3:c.11569A>T	XP_005248319.2:p.Thr3857Ser
XM_017009177.1:c.11569A>T	XP_016864666.1:p.Thr3857Ser
XM_017009178.1:c.10474A>T	XP_016864667.1:p.Thr3492Ser
XM_017009179.2:c.10474A>T	XP_016864668.1:p.Thr3492Ser
XM_017009180.1:c.11569A>T	XP_016864669.1:p.Thr3857Ser
XM_017009181.1:c.11569A>T	XP_016864670.1:p.Thr3857Ser
XM_017009182.1:c.11325A>T	XP_016864671.1:p.Leu3775=
XM_017009185.1:c.6658A>T	XP_016864674.1:p.Thr2220Ser
XM_017009186.1:c.6211A>T	XP_016864675.1:p.Thr2071Ser
XM_017009188.1:c.5548A>T	XP_016864677.1:p.Thr1850Ser
XM_024454388.1:c.10474A>T	XP_024310156.1:p.Thr3492Ser
XM_024454389.1:c.10063A>T	XP_024310157.1:p.Thr3355Ser
NM_001369.3:c.11461A>T MANE Select	NP_001360.1:p.Thr3821Ser