Canonical Allele Identifier: CA359188580

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692142G>A (hg19) ; chr5:g.13692033G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692033G>A , CM000667.2:g.13692033G>A	GRCh38
NC_000005.9:g.13692142G>A , CM000667.1:g.13692142G>A	GRCh37
NC_000005.8:g.13745142G>A	NCBI36
NG_013081.1:g.257448C>T
NG_013081.2:g.257448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1159C>T
ENST00000265104.5:c.13826C>T MANE Select	ENSP00000265104.4:p.Pro4609Leu
ENST00000681290.1:c.13781C>T	ENSP00000505288.1:p.Pro4594Leu
ENST00000265104.4:c.13826C>T	ENSP00000265104.4:p.Pro4609Leu
NM_001369.2:c.13826C>T	NP_001360.1:p.Pro4609Leu
XM_005248262.2:c.13781C>T	XP_005248319.1:p.Pro4594Leu
XM_005248262.3:c.13934C>T	XP_005248319.2:p.Pro4645Leu
XM_017009177.1:c.13514C>T	XP_016864666.1:p.Pro4505Leu
XM_017009178.1:c.12839C>T	XP_016864667.1:p.Pro4280Leu
XM_017009179.2:c.12839C>T	XP_016864668.1:p.Pro4280Leu
XM_017009185.1:c.9023C>T	XP_016864674.1:p.Pro3008Leu
XM_017009186.1:c.8576C>T	XP_016864675.1:p.Pro2859Leu
XM_017009188.1:c.7913C>T	XP_016864677.1:p.Pro2638Leu
XM_024454388.1:c.12839C>T	XP_024310156.1:p.Pro4280Leu
XM_024454389.1:c.12428C>T	XP_024310157.1:p.Pro4143Leu
NM_001369.3:c.13826C>T MANE Select	NP_001360.1:p.Pro4609Leu