Canonical Allele Identifier: CA359192192

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13753609G>C (hg19) ; chr5:g.13753500G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753500G>C , CM000667.2:g.13753500G>C	GRCh38
NC_000005.9:g.13753609G>C , CM000667.1:g.13753609G>C	GRCh37
NC_000005.8:g.13806609G>C	NCBI36
NG_013081.1:g.195981C>G
NG_013081.2:g.195981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10605C>G MANE Select	ENSP00000265104.4:p.Asn3535Lys
ENST00000681290.1:c.10560C>G	ENSP00000505288.1:p.Asn3520Lys
ENST00000265104.4:c.10605C>G	ENSP00000265104.4:p.Asn3535Lys
NM_001369.2:c.10605C>G	NP_001360.1:p.Asn3535Lys
XM_005248262.2:c.10560C>G	XP_005248319.1:p.Asn3520Lys
XM_005248262.3:c.10713C>G	XP_005248319.2:p.Asn3571Lys
XM_017009177.1:c.10713C>G	XP_016864666.1:p.Asn3571Lys
XM_017009178.1:c.9618C>G	XP_016864667.1:p.Asn3206Lys
XM_017009179.2:c.9618C>G	XP_016864668.1:p.Asn3206Lys
XM_017009180.1:c.10713C>G	XP_016864669.1:p.Asn3571Lys
XM_017009181.1:c.10713C>G	XP_016864670.1:p.Asn3571Lys
XM_017009182.1:c.10713C>G	XP_016864671.1:p.Asn3571Lys
XM_017009185.1:c.5802C>G	XP_016864674.1:p.Asn1934Lys
XM_017009186.1:c.5355C>G	XP_016864675.1:p.Asn1785Lys
XM_017009188.1:c.4692C>G	XP_016864677.1:p.Asn1564Lys
XM_024454388.1:c.9618C>G	XP_024310156.1:p.Asn3206Lys
XM_024454389.1:c.9207C>G	XP_024310157.1:p.Asn3069Lys
NM_001369.3:c.10605C>G MANE Select	NP_001360.1:p.Asn3535Lys