Canonical Allele Identifier: CA113949102

Gene: DNAH5

Linked Data

• dbSNP Id: rs923601318
• gnomAD v3: 5-13780980-A-G
• gnomAD v4: 5-13780980-A-G
• MyVariant Identifiers: chr5:g.13781089A>G (hg19) ; chr5:g.13780980A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780980A>G , CM000667.2:g.13780980A>G	GRCh38
NC_000005.9:g.13781089A>G , CM000667.1:g.13781089A>G	GRCh37
NC_000005.8:g.13834089A>G	NCBI36
NG_013081.1:g.168501T>C
NG_013081.2:g.168501T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8821-21T>C MANE Select	ENSP00000265104.4:n.8821-21T>C
ENST00000681290.1:c.8776-21T>C	ENSP00000505288.1:n.8776-21T>C
ENST00000265104.4:c.8821-21T>C	ENSP00000265104.4:n.8821-21T>C
NM_001369.2:c.8821-21T>C	NP_001360.1:n.8821-21T>C
XM_005248262.2:c.8776-21T>C	XP_005248319.1:n.8776-21T>C
XM_011513990.1:c.8821-21T>C	XP_011512292.1:n.8821-21T>C
XR_925598.1:n.9028-3625T>C
XM_005248262.3:c.8929-21T>C	XP_005248319.2:n.8929-21T>C
XM_017009177.1:c.8929-21T>C	XP_016864666.1:n.8929-21T>C
XM_017009178.1:c.7834-21T>C	XP_016864667.1:n.7834-21T>C
XM_017009179.2:c.7834-21T>C	XP_016864668.1:n.7834-21T>C
XM_017009180.1:c.8929-21T>C	XP_016864669.1:n.8929-21T>C
XM_017009181.1:c.8929-21T>C	XP_016864670.1:n.8929-21T>C
XM_017009182.1:c.8929-21T>C	XP_016864671.1:n.8929-21T>C
XM_017009183.1:c.8929-21T>C	XP_016864672.1:n.8929-21T>C
XM_017009184.1:c.8929-21T>C	XP_016864673.1:n.8929-21T>C
XM_017009185.1:c.4018-21T>C	XP_016864674.1:n.4018-21T>C
XM_017009186.1:c.3571-21T>C	XP_016864675.1:n.3571-21T>C
XM_017009188.1:c.2908-21T>C	XP_016864677.1:n.2908-21T>C
XM_024454388.1:c.7834-21T>C	XP_024310156.1:n.7834-21T>C
XM_024454389.1:c.7423-21T>C	XP_024310157.1:n.7423-21T>C
XR_001742034.1:n.8946-3625T>C
XR_001742035.1:n.8946-3625T>C
NM_001369.3:c.8821-21T>C MANE Select	NP_001360.1:n.8821-21T>C