Canonical Allele Identifier: CA804449843

Gene: DNAH5

Linked Data

• dbSNP Id: rs534432707
• MyVariant Identifiers: chr5:g.13769357_13769358insG (hg19) ; chr5:g.13769248_13769249insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769248_13769249insG , CM000667.2:g.13769248_13769249insG	GRCh38
NC_000005.9:g.13769357_13769358insG , CM000667.1:g.13769357_13769358insG	GRCh37
NC_000005.8:g.13822357_13822358insG	NCBI36
NG_013081.1:g.180232_180233insC
NG_013081.2:g.180232_180233insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-113_9721-112insC MANE Select	ENSP00000265104.4:n.9721-113_9721-112insC
ENST00000681290.1:c.9676-113_9676-112insC	ENSP00000505288.1:n.9676-113_9676-112insC
ENST00000265104.4:c.9721-113_9721-112insC	ENSP00000265104.4:n.9721-113_9721-112insC
ENST00000504001.3:n.433-113_433-112insC
NM_001369.2:c.9721-113_9721-112insC	NP_001360.1:n.9721-113_9721-112insC
XM_005248262.2:c.9676-113_9676-112insC	XP_005248319.1:n.9676-113_9676-112insC
XM_005248262.3:c.9829-113_9829-112insC	XP_005248319.2:n.9829-113_9829-112insC
XM_017009177.1:c.9829-113_9829-112insC	XP_016864666.1:n.9829-113_9829-112insC
XM_017009178.1:c.8734-113_8734-112insC	XP_016864667.1:n.8734-113_8734-112insC
XM_017009179.2:c.8734-113_8734-112insC	XP_016864668.1:n.8734-113_8734-112insC
XM_017009180.1:c.9829-113_9829-112insC	XP_016864669.1:n.9829-113_9829-112insC
XM_017009181.1:c.9829-113_9829-112insC	XP_016864670.1:n.9829-113_9829-112insC
XM_017009182.1:c.9829-113_9829-112insC	XP_016864671.1:n.9829-113_9829-112insC
XM_017009185.1:c.4918-113_4918-112insC	XP_016864674.1:n.4918-113_4918-112insC
XM_017009186.1:c.4471-113_4471-112insC	XP_016864675.1:n.4471-113_4471-112insC
XM_017009188.1:c.3808-113_3808-112insC	XP_016864677.1:n.3808-113_3808-112insC
XM_024454388.1:c.8734-113_8734-112insC	XP_024310156.1:n.8734-113_8734-112insC
XM_024454389.1:c.8323-113_8323-112insC	XP_024310157.1:n.8323-113_8323-112insC
NM_001369.3:c.9721-113_9721-112insC MANE Select	NP_001360.1:n.9721-113_9721-112insC