Canonical Allele Identifier: CA359188600

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692152C>T (hg19) ; chr5:g.13692043C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692043C>T , CM000667.2:g.13692043C>T	GRCh38
NC_000005.9:g.13692152C>T , CM000667.1:g.13692152C>T	GRCh37
NC_000005.8:g.13745152C>T	NCBI36
NG_013081.1:g.257438G>A
NG_013081.2:g.257438G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.1149G>A
ENST00000265104.5:c.13816G>A MANE Select	ENSP00000265104.4:p.Ala4606Thr
ENST00000681290.1:c.13771G>A	ENSP00000505288.1:p.Ala4591Thr
ENST00000265104.4:c.13816G>A	ENSP00000265104.4:p.Ala4606Thr
NM_001369.2:c.13816G>A	NP_001360.1:p.Ala4606Thr
XM_005248262.2:c.13771G>A	XP_005248319.1:p.Ala4591Thr
XM_005248262.3:c.13924G>A	XP_005248319.2:p.Ala4642Thr
XM_017009177.1:c.13504G>A	XP_016864666.1:p.Ala4502Thr
XM_017009178.1:c.12829G>A	XP_016864667.1:p.Ala4277Thr
XM_017009179.2:c.12829G>A	XP_016864668.1:p.Ala4277Thr
XM_017009185.1:c.9013G>A	XP_016864674.1:p.Ala3005Thr
XM_017009186.1:c.8566G>A	XP_016864675.1:p.Ala2856Thr
XM_017009188.1:c.7903G>A	XP_016864677.1:p.Ala2635Thr
XM_024454388.1:c.12829G>A	XP_024310156.1:p.Ala4277Thr
XM_024454389.1:c.12418G>A	XP_024310157.1:p.Ala4140Thr
NM_001369.3:c.13816G>A MANE Select	NP_001360.1:p.Ala4606Thr