Canonical Allele Identifier: CA359188684

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692196A>G (hg19) ; chr5:g.13692087A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692087A>G , CM000667.2:g.13692087A>G	GRCh38
NC_000005.9:g.13692196A>G , CM000667.1:g.13692196A>G	GRCh37
NC_000005.8:g.13745196A>G	NCBI36
NG_013081.1:g.257394T>C
NG_013081.2:g.257394T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1105T>C
ENST00000265104.5:c.13772T>C MANE Select	ENSP00000265104.4:p.Val4591Ala
ENST00000681290.1:c.13727T>C	ENSP00000505288.1:p.Val4576Ala
ENST00000265104.4:c.13772T>C	ENSP00000265104.4:p.Val4591Ala
NM_001369.2:c.13772T>C	NP_001360.1:p.Val4591Ala
XM_005248262.2:c.13727T>C	XP_005248319.1:p.Val4576Ala
XM_005248262.3:c.13880T>C	XP_005248319.2:p.Val4627Ala
XM_017009177.1:c.13460T>C	XP_016864666.1:p.Val4487Ala
XM_017009178.1:c.12785T>C	XP_016864667.1:p.Val4262Ala
XM_017009179.2:c.12785T>C	XP_016864668.1:p.Val4262Ala
XM_017009185.1:c.8969T>C	XP_016864674.1:p.Val2990Ala
XM_017009186.1:c.8522T>C	XP_016864675.1:p.Val2841Ala
XM_017009188.1:c.7859T>C	XP_016864677.1:p.Val2620Ala
XM_024454388.1:c.12785T>C	XP_024310156.1:p.Val4262Ala
XM_024454389.1:c.12374T>C	XP_024310157.1:p.Val4125Ala
NM_001369.3:c.13772T>C MANE Select	NP_001360.1:p.Val4591Ala