Canonical Allele Identifier: CA2673269821

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13769251-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769251_13769252insG , CM000667.2:g.13769251_13769252insG	GRCh38
NC_000005.9:g.13769360_13769361insG , CM000667.1:g.13769360_13769361insG	GRCh37
NC_000005.8:g.13822360_13822361insG	NCBI36
NG_013081.1:g.180229_180230insC
NG_013081.2:g.180229_180230insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-116_9721-115insC MANE Select	ENSP00000265104.4:n.9721-116_9721-115insC
ENST00000681290.1:c.9676-116_9676-115insC	ENSP00000505288.1:n.9676-116_9676-115insC
ENST00000265104.4:c.9721-116_9721-115insC	ENSP00000265104.4:n.9721-116_9721-115insC
ENST00000504001.3:n.433-116_433-115insC
NM_001369.2:c.9721-116_9721-115insC	NP_001360.1:n.9721-116_9721-115insC
XM_005248262.2:c.9676-116_9676-115insC	XP_005248319.1:n.9676-116_9676-115insC
XM_005248262.3:c.9829-116_9829-115insC	XP_005248319.2:n.9829-116_9829-115insC
XM_017009177.1:c.9829-116_9829-115insC	XP_016864666.1:n.9829-116_9829-115insC
XM_017009178.1:c.8734-116_8734-115insC	XP_016864667.1:n.8734-116_8734-115insC
XM_017009179.2:c.8734-116_8734-115insC	XP_016864668.1:n.8734-116_8734-115insC
XM_017009180.1:c.9829-116_9829-115insC	XP_016864669.1:n.9829-116_9829-115insC
XM_017009181.1:c.9829-116_9829-115insC	XP_016864670.1:n.9829-116_9829-115insC
XM_017009182.1:c.9829-116_9829-115insC	XP_016864671.1:n.9829-116_9829-115insC
XM_017009185.1:c.4918-116_4918-115insC	XP_016864674.1:n.4918-116_4918-115insC
XM_017009186.1:c.4471-116_4471-115insC	XP_016864675.1:n.4471-116_4471-115insC
XM_017009188.1:c.3808-116_3808-115insC	XP_016864677.1:n.3808-116_3808-115insC
XM_024454388.1:c.8734-116_8734-115insC	XP_024310156.1:n.8734-116_8734-115insC
XM_024454389.1:c.8323-116_8323-115insC	XP_024310157.1:n.8323-116_8323-115insC
NM_001369.3:c.9721-116_9721-115insC MANE Select	NP_001360.1:n.9721-116_9721-115insC