Canonical Allele Identifier: CA443535717

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13776488-T-A
• MyVariant Identifiers: chr5:g.13776597T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776488T>A , CM000667.2:g.13776488T>A	GRCh38
NC_000005.9:g.13776597T>A , CM000667.1:g.13776597T>A	GRCh37
NC_000005.8:g.13829597T>A	NCBI36
NG_013081.1:g.172993A>T
NG_013081.2:g.172993A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9324A>T MANE Select	ENSP00000265104.4:p.Gly3108=
ENST00000681290.1:c.9279A>T	ENSP00000505288.1:p.Gly3093=
ENST00000265104.4:c.9324A>T	ENSP00000265104.4:p.Gly3108=
NM_001369.2:c.9324A>T	NP_001360.1:p.Gly3108=
XM_005248262.2:c.9279A>T	XP_005248319.1:p.Gly3093=
XM_005248262.3:c.9432A>T	XP_005248319.2:p.Gly3144=
XM_017009177.1:c.9432A>T	XP_016864666.1:p.Gly3144=
XM_017009178.1:c.8337A>T	XP_016864667.1:p.Gly2779=
XM_017009179.2:c.8337A>T	XP_016864668.1:p.Gly2779=
XM_017009180.1:c.9432A>T	XP_016864669.1:p.Gly3144=
XM_017009181.1:c.9432A>T	XP_016864670.1:p.Gly3144=
XM_017009182.1:c.9432A>T	XP_016864671.1:p.Gly3144=
XM_017009183.1:c.9432A>T	XP_016864672.1:p.Gly3144=
XM_017009185.1:c.4521A>T	XP_016864674.1:p.Gly1507=
XM_017009186.1:c.4074A>T	XP_016864675.1:p.Gly1358=
XM_017009188.1:c.3411A>T	XP_016864677.1:p.Gly1137=
XM_024454388.1:c.8337A>T	XP_024310156.1:p.Gly2779=
XM_024454389.1:c.7926A>T	XP_024310157.1:p.Gly2642=
NM_001369.3:c.9324A>T MANE Select	NP_001360.1:p.Gly3108=