Canonical Allele Identifier: CA557870075

Gene: DNAH5

Linked Data

• dbSNP Id: rs1305532463
• gnomAD v2: 5-13769362-T-TG
• gnomAD v3: 5-13769253-T-TG
• gnomAD v4: 5-13769253-T-TG
• MyVariant Identifiers: chr5:g.13769362_13769363insG (hg19) ; chr5:g.13769253_13769254insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769253_13769254insG , CM000667.2:g.13769253_13769254insG	GRCh38
NC_000005.9:g.13769362_13769363insG , CM000667.1:g.13769362_13769363insG	GRCh37
NC_000005.8:g.13822362_13822363insG	NCBI36
NG_013081.1:g.180227_180228insC
NG_013081.2:g.180227_180228insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-118_9721-117insC MANE Select	ENSP00000265104.4:n.9721-118_9721-117insC
ENST00000681290.1:c.9676-118_9676-117insC	ENSP00000505288.1:n.9676-118_9676-117insC
ENST00000265104.4:c.9721-118_9721-117insC	ENSP00000265104.4:n.9721-118_9721-117insC
ENST00000504001.3:n.433-118_433-117insC
NM_001369.2:c.9721-118_9721-117insC	NP_001360.1:n.9721-118_9721-117insC
XM_005248262.2:c.9676-118_9676-117insC	XP_005248319.1:n.9676-118_9676-117insC
XM_005248262.3:c.9829-118_9829-117insC	XP_005248319.2:n.9829-118_9829-117insC
XM_017009177.1:c.9829-118_9829-117insC	XP_016864666.1:n.9829-118_9829-117insC
XM_017009178.1:c.8734-118_8734-117insC	XP_016864667.1:n.8734-118_8734-117insC
XM_017009179.2:c.8734-118_8734-117insC	XP_016864668.1:n.8734-118_8734-117insC
XM_017009180.1:c.9829-118_9829-117insC	XP_016864669.1:n.9829-118_9829-117insC
XM_017009181.1:c.9829-118_9829-117insC	XP_016864670.1:n.9829-118_9829-117insC
XM_017009182.1:c.9829-118_9829-117insC	XP_016864671.1:n.9829-118_9829-117insC
XM_017009185.1:c.4918-118_4918-117insC	XP_016864674.1:n.4918-118_4918-117insC
XM_017009186.1:c.4471-118_4471-117insC	XP_016864675.1:n.4471-118_4471-117insC
XM_017009188.1:c.3808-118_3808-117insC	XP_016864677.1:n.3808-118_3808-117insC
XM_024454388.1:c.8734-118_8734-117insC	XP_024310156.1:n.8734-118_8734-117insC
XM_024454389.1:c.8323-118_8323-117insC	XP_024310157.1:n.8323-118_8323-117insC
NM_001369.3:c.9721-118_9721-117insC MANE Select	NP_001360.1:n.9721-118_9721-117insC