Canonical Allele Identifier: CA359204468

Gene: DNAH5

Linked Data

• dbSNP Id: rs1417478346
• gnomAD v2: 5-13770930-T-C
• gnomAD v4: 5-13770821-T-C
• MyVariant Identifiers: chr5:g.13770930T>C (hg19) ; chr5:g.13770821T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770821T>C , CM000667.2:g.13770821T>C	GRCh38
NC_000005.9:g.13770930T>C , CM000667.1:g.13770930T>C	GRCh37
NC_000005.8:g.13823930T>C	NCBI36
NG_013081.1:g.178660A>G
NG_013081.2:g.178660A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9533A>G MANE Select	ENSP00000265104.4:p.Tyr3178Cys
ENST00000681290.1:c.9488A>G	ENSP00000505288.1:p.Tyr3163Cys
ENST00000265104.4:c.9533A>G	ENSP00000265104.4:p.Tyr3178Cys
ENST00000504001.3:n.245A>G
NM_001369.2:c.9533A>G	NP_001360.1:p.Tyr3178Cys
XM_005248262.2:c.9488A>G	XP_005248319.1:p.Tyr3163Cys
XM_005248262.3:c.9641A>G	XP_005248319.2:p.Tyr3214Cys
XM_017009177.1:c.9641A>G	XP_016864666.1:p.Tyr3214Cys
XM_017009178.1:c.8546A>G	XP_016864667.1:p.Tyr2849Cys
XM_017009179.2:c.8546A>G	XP_016864668.1:p.Tyr2849Cys
XM_017009180.1:c.9641A>G	XP_016864669.1:p.Tyr3214Cys
XM_017009181.1:c.9641A>G	XP_016864670.1:p.Tyr3214Cys
XM_017009182.1:c.9641A>G	XP_016864671.1:p.Tyr3214Cys
XM_017009183.1:c.9641A>G	XP_016864672.1:p.Tyr3214Cys
XM_017009185.1:c.4730A>G	XP_016864674.1:p.Tyr1577Cys
XM_017009186.1:c.4283A>G	XP_016864675.1:p.Tyr1428Cys
XM_017009188.1:c.3620A>G	XP_016864677.1:p.Tyr1207Cys
XM_024454388.1:c.8546A>G	XP_024310156.1:p.Tyr2849Cys
XM_024454389.1:c.8135A>G	XP_024310157.1:p.Tyr2712Cys
NM_001369.3:c.9533A>G MANE Select	NP_001360.1:p.Tyr3178Cys