Canonical Allele Identifier: CA359221816

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13794061T>G (hg19) ; chr5:g.13793952T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13793952T>G , CM000667.2:g.13793952T>G	GRCh38
NC_000005.9:g.13794061T>G , CM000667.1:g.13794061T>G	GRCh37
NC_000005.8:g.13847061T>G	NCBI36
NG_013081.1:g.155529A>C
NG_013081.2:g.155529A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.7994A>C MANE Select	ENSP00000265104.4:p.Asn2665Thr
ENST00000681290.1:c.7949A>C	ENSP00000505288.1:p.Asn2650Thr
ENST00000265104.4:c.7994A>C	ENSP00000265104.4:p.Asn2665Thr
NM_001369.2:c.7994A>C	NP_001360.1:p.Asn2665Thr
XM_005248262.2:c.7949A>C	XP_005248319.1:p.Asn2650Thr
XM_011513990.1:c.7994A>C	XP_011512292.1:p.Asn2665Thr
XR_925598.1:n.8201A>C
XM_005248262.3:c.8102A>C	XP_005248319.2:p.Asn2701Thr
XM_017009177.1:c.8102A>C	XP_016864666.1:p.Asn2701Thr
XM_017009178.1:c.7007A>C	XP_016864667.1:p.Asn2336Thr
XM_017009179.2:c.7007A>C	XP_016864668.1:p.Asn2336Thr
XM_017009180.1:c.8102A>C	XP_016864669.1:p.Asn2701Thr
XM_017009181.1:c.8102A>C	XP_016864670.1:p.Asn2701Thr
XM_017009182.1:c.8102A>C	XP_016864671.1:p.Asn2701Thr
XM_017009183.1:c.8102A>C	XP_016864672.1:p.Asn2701Thr
XM_017009184.1:c.8102A>C	XP_016864673.1:p.Asn2701Thr
XM_017009185.1:c.3191A>C	XP_016864674.1:p.Asn1064Thr
XM_017009186.1:c.2744A>C	XP_016864675.1:p.Asn915Thr
XM_017009188.1:c.2081A>C	XP_016864677.1:p.Asn694Thr
XM_024454388.1:c.7007A>C	XP_024310156.1:p.Asn2336Thr
XM_024454389.1:c.6596A>C	XP_024310157.1:p.Asn2199Thr
XR_001742034.1:n.8119A>C
XR_001742035.1:n.8119A>C
NM_001369.3:c.7994A>C MANE Select	NP_001360.1:p.Asn2665Thr