Canonical Allele Identifier: CA359188772

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692236C>G (hg19) ; chr5:g.13692127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692127C>G , CM000667.2:g.13692127C>G	GRCh38
NC_000005.9:g.13692236C>G , CM000667.1:g.13692236C>G	GRCh37
NC_000005.8:g.13745236C>G	NCBI36
NG_013081.1:g.257354G>C
NG_013081.2:g.257354G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1065G>C
ENST00000265104.5:c.13732G>C MANE Select	ENSP00000265104.4:p.Asp4578His
ENST00000681290.1:c.13687G>C	ENSP00000505288.1:p.Asp4563His
ENST00000265104.4:c.13732G>C	ENSP00000265104.4:p.Asp4578His
NM_001369.2:c.13732G>C	NP_001360.1:p.Asp4578His
XM_005248262.2:c.13687G>C	XP_005248319.1:p.Asp4563His
XM_005248262.3:c.13840G>C	XP_005248319.2:p.Asp4614His
XM_017009177.1:c.13420G>C	XP_016864666.1:p.Asp4474His
XM_017009178.1:c.12745G>C	XP_016864667.1:p.Asp4249His
XM_017009179.2:c.12745G>C	XP_016864668.1:p.Asp4249His
XM_017009185.1:c.8929G>C	XP_016864674.1:p.Asp2977His
XM_017009186.1:c.8482G>C	XP_016864675.1:p.Asp2828His
XM_017009188.1:c.7819G>C	XP_016864677.1:p.Asp2607His
XM_024454388.1:c.12745G>C	XP_024310156.1:p.Asp4249His
XM_024454389.1:c.12334G>C	XP_024310157.1:p.Asp4112His
NM_001369.3:c.13732G>C MANE Select	NP_001360.1:p.Asp4578His