Canonical Allele Identifier: CA359197427

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708365C>G (hg19) ; chr5:g.13708256C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708256C>G , CM000667.2:g.13708256C>G	GRCh38
NC_000005.9:g.13708365C>G , CM000667.1:g.13708365C>G	GRCh37
NC_000005.8:g.13761365C>G	NCBI36
NG_013081.1:g.241225G>C
NG_013081.2:g.241225G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.538G>C
ENST00000265104.5:c.13205G>C MANE Select	ENSP00000265104.4:p.Arg4402Thr
ENST00000681290.1:c.13160G>C	ENSP00000505288.1:p.Arg4387Thr
ENST00000265104.4:c.13205G>C	ENSP00000265104.4:p.Arg4402Thr
NM_001369.2:c.13205G>C	NP_001360.1:p.Arg4402Thr
XM_005248262.2:c.13160G>C	XP_005248319.1:p.Arg4387Thr
XM_005248262.3:c.13313G>C	XP_005248319.2:p.Arg4438Thr
XM_017009177.1:c.12893G>C	XP_016864666.1:p.Arg4298Thr
XM_017009178.1:c.12218G>C	XP_016864667.1:p.Arg4073Thr
XM_017009179.2:c.12218G>C	XP_016864668.1:p.Arg4073Thr
XM_017009185.1:c.8402G>C	XP_016864674.1:p.Arg2801Thr
XM_017009186.1:c.7955G>C	XP_016864675.1:p.Arg2652Thr
XM_017009188.1:c.7292G>C	XP_016864677.1:p.Arg2431Thr
XM_024454388.1:c.12218G>C	XP_024310156.1:p.Arg4073Thr
XM_024454389.1:c.11807G>C	XP_024310157.1:p.Arg3936Thr
NM_001369.3:c.13205G>C MANE Select	NP_001360.1:p.Arg4402Thr