Canonical Allele Identifier: CA359208251

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13776614G>T (hg19) ; chr5:g.13776505G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13776505G>T , CM000667.2:g.13776505G>T	GRCh38
NC_000005.9:g.13776614G>T , CM000667.1:g.13776614G>T	GRCh37
NC_000005.8:g.13829614G>T	NCBI36
NG_013081.1:g.172976C>A
NG_013081.2:g.172976C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9307C>A MANE Select	ENSP00000265104.4:p.Pro3103Thr
ENST00000681290.1:c.9262C>A	ENSP00000505288.1:p.Pro3088Thr
ENST00000265104.4:c.9307C>A	ENSP00000265104.4:p.Pro3103Thr
NM_001369.2:c.9307C>A	NP_001360.1:p.Pro3103Thr
XM_005248262.2:c.9262C>A	XP_005248319.1:p.Pro3088Thr
XM_005248262.3:c.9415C>A	XP_005248319.2:p.Pro3139Thr
XM_017009177.1:c.9415C>A	XP_016864666.1:p.Pro3139Thr
XM_017009178.1:c.8320C>A	XP_016864667.1:p.Pro2774Thr
XM_017009179.2:c.8320C>A	XP_016864668.1:p.Pro2774Thr
XM_017009180.1:c.9415C>A	XP_016864669.1:p.Pro3139Thr
XM_017009181.1:c.9415C>A	XP_016864670.1:p.Pro3139Thr
XM_017009182.1:c.9415C>A	XP_016864671.1:p.Pro3139Thr
XM_017009183.1:c.9415C>A	XP_016864672.1:p.Pro3139Thr
XM_017009185.1:c.4504C>A	XP_016864674.1:p.Pro1502Thr
XM_017009186.1:c.4057C>A	XP_016864675.1:p.Pro1353Thr
XM_017009188.1:c.3394C>A	XP_016864677.1:p.Pro1132Thr
XM_024454388.1:c.8320C>A	XP_024310156.1:p.Pro2774Thr
XM_024454389.1:c.7909C>A	XP_024310157.1:p.Pro2637Thr
NM_001369.3:c.9307C>A MANE Select	NP_001360.1:p.Pro3103Thr