Canonical Allele Identifier: CA443251366

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13829655C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829546C>G , CM000667.2:g.13829546C>G	GRCh38
NC_000005.9:g.13829655C>G , CM000667.1:g.13829655C>G	GRCh37
NC_000005.8:g.13882655C>G	NCBI36
NG_013081.1:g.119935G>C
NG_013081.2:g.119935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.1339G>C
ENST00000265104.5:c.6408G>C MANE Select	ENSP00000265104.4:p.Thr2136=
ENST00000681290.1:c.6363G>C	ENSP00000505288.1:p.Thr2121=
ENST00000265104.4:c.6408G>C	ENSP00000265104.4:p.Thr2136=
NM_001369.2:c.6408G>C	NP_001360.1:p.Thr2136=
XM_005248262.2:c.6363G>C	XP_005248319.1:p.Thr2121=
XM_011513990.1:c.6408G>C	XP_011512292.1:p.Thr2136=
XR_925598.1:n.6615G>C
XM_005248262.3:c.6516G>C	XP_005248319.2:p.Thr2172=
XM_017009177.1:c.6516G>C	XP_016864666.1:p.Thr2172=
XM_017009178.1:c.5421G>C	XP_016864667.1:p.Thr1807=
XM_017009179.2:c.5421G>C	XP_016864668.1:p.Thr1807=
XM_017009180.1:c.6516G>C	XP_016864669.1:p.Thr2172=
XM_017009181.1:c.6516G>C	XP_016864670.1:p.Thr2172=
XM_017009182.1:c.6516G>C	XP_016864671.1:p.Thr2172=
XM_017009183.1:c.6516G>C	XP_016864672.1:p.Thr2172=
XM_017009184.1:c.6516G>C	XP_016864673.1:p.Thr2172=
XM_017009185.1:c.1605G>C	XP_016864674.1:p.Thr535=
XM_017009186.1:c.1158G>C	XP_016864675.1:p.Thr386=
XM_017009187.1:c.6516G>C	XP_016864676.1:p.Thr2172=
XM_017009188.1:c.495G>C	XP_016864677.1:p.Thr165=
XM_024454388.1:c.5421G>C	XP_024310156.1:p.Thr1807=
XM_024454389.1:c.5010G>C	XP_024310157.1:p.Thr1670=
XR_001742034.1:n.6533G>C
XR_001742035.1:n.6533G>C
NM_001369.3:c.6408G>C MANE Select	NP_001360.1:p.Thr2136=