Canonical Allele Identifier: CA359207174

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717509T>G (hg19) ; chr5:g.13717400T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717400T>G , CM000667.2:g.13717400T>G	GRCh38
NC_000005.9:g.13717509T>G , CM000667.1:g.13717509T>G	GRCh37
NC_000005.8:g.13770509T>G	NCBI36
NG_013081.1:g.232081A>C
NG_013081.2:g.232081A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12620A>C MANE Select	ENSP00000265104.4:p.Asn4207Thr
ENST00000681290.1:c.12575A>C	ENSP00000505288.1:p.Asn4192Thr
ENST00000265104.4:c.12620A>C	ENSP00000265104.4:p.Asn4207Thr
NM_001369.2:c.12620A>C	NP_001360.1:p.Asn4207Thr
XM_005248262.2:c.12575A>C	XP_005248319.1:p.Asn4192Thr
XM_005248262.3:c.12728A>C	XP_005248319.2:p.Asn4243Thr
XM_017009177.1:c.12728A>C	XP_016864666.1:p.Asn4243Thr
XM_017009178.1:c.11633A>C	XP_016864667.1:p.Asn3878Thr
XM_017009179.2:c.11633A>C	XP_016864668.1:p.Asn3878Thr
XM_017009180.1:c.12728A>C	XP_016864669.1:p.Asn4243Thr
XM_017009185.1:c.7817A>C	XP_016864674.1:p.Asn2606Thr
XM_017009186.1:c.7370A>C	XP_016864675.1:p.Asn2457Thr
XM_017009188.1:c.6707A>C	XP_016864677.1:p.Asn2236Thr
XM_024454388.1:c.11633A>C	XP_024310156.1:p.Asn3878Thr
XM_024454389.1:c.11222A>C	XP_024310157.1:p.Asn3741Thr
NM_001369.3:c.12620A>C MANE Select	NP_001360.1:p.Asn4207Thr