Canonical Allele Identifier: CA3202178

Gene: DNAH5

Linked Data

• dbSNP Id: rs750988827
• ExAC: 5:13753650 G / C
• MyVariant Identifiers: chr5:g.13753650G>C (hg19) ; chr5:g.13753541G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753541G>C , CM000667.2:g.13753541G>C	GRCh38
NC_000005.9:g.13753650G>C , CM000667.1:g.13753650G>C	GRCh37
NC_000005.8:g.13806650G>C	NCBI36
NG_013081.1:g.195940C>G
NG_013081.2:g.195940C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10564C>G MANE Select	ENSP00000265104.4:p.Leu3522Val
ENST00000681290.1:c.10519C>G	ENSP00000505288.1:p.Leu3507Val
ENST00000265104.4:c.10564C>G	ENSP00000265104.4:p.Leu3522Val
NM_001369.2:c.10564C>G	NP_001360.1:p.Leu3522Val
XM_005248262.2:c.10519C>G	XP_005248319.1:p.Leu3507Val
XM_005248262.3:c.10672C>G	XP_005248319.2:p.Leu3558Val
XM_017009177.1:c.10672C>G	XP_016864666.1:p.Leu3558Val
XM_017009178.1:c.9577C>G	XP_016864667.1:p.Leu3193Val
XM_017009179.2:c.9577C>G	XP_016864668.1:p.Leu3193Val
XM_017009180.1:c.10672C>G	XP_016864669.1:p.Leu3558Val
XM_017009181.1:c.10672C>G	XP_016864670.1:p.Leu3558Val
XM_017009182.1:c.10672C>G	XP_016864671.1:p.Leu3558Val
XM_017009185.1:c.5761C>G	XP_016864674.1:p.Leu1921Val
XM_017009186.1:c.5314C>G	XP_016864675.1:p.Leu1772Val
XM_017009188.1:c.4651C>G	XP_016864677.1:p.Leu1551Val
XM_024454388.1:c.9577C>G	XP_024310156.1:p.Leu3193Val
XM_024454389.1:c.9166C>G	XP_024310157.1:p.Leu3056Val
NM_001369.3:c.10564C>G MANE Select	NP_001360.1:p.Leu3522Val