Canonical Allele Identifier: CA359188652

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692178T>G (hg19) ; chr5:g.13692069T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692069T>G , CM000667.2:g.13692069T>G	GRCh38
NC_000005.9:g.13692178T>G , CM000667.1:g.13692178T>G	GRCh37
NC_000005.8:g.13745178T>G	NCBI36
NG_013081.1:g.257412A>C
NG_013081.2:g.257412A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1123A>C
ENST00000265104.5:c.13790A>C MANE Select	ENSP00000265104.4:p.Tyr4597Ser
ENST00000681290.1:c.13745A>C	ENSP00000505288.1:p.Tyr4582Ser
ENST00000265104.4:c.13790A>C	ENSP00000265104.4:p.Tyr4597Ser
NM_001369.2:c.13790A>C	NP_001360.1:p.Tyr4597Ser
XM_005248262.2:c.13745A>C	XP_005248319.1:p.Tyr4582Ser
XM_005248262.3:c.13898A>C	XP_005248319.2:p.Tyr4633Ser
XM_017009177.1:c.13478A>C	XP_016864666.1:p.Tyr4493Ser
XM_017009178.1:c.12803A>C	XP_016864667.1:p.Tyr4268Ser
XM_017009179.2:c.12803A>C	XP_016864668.1:p.Tyr4268Ser
XM_017009185.1:c.8987A>C	XP_016864674.1:p.Tyr2996Ser
XM_017009186.1:c.8540A>C	XP_016864675.1:p.Tyr2847Ser
XM_017009188.1:c.7877A>C	XP_016864677.1:p.Tyr2626Ser
XM_024454388.1:c.12803A>C	XP_024310156.1:p.Tyr4268Ser
XM_024454389.1:c.12392A>C	XP_024310157.1:p.Tyr4131Ser
NM_001369.3:c.13790A>C MANE Select	NP_001360.1:p.Tyr4597Ser