Canonical Allele Identifier: CA359207469

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13717531T>G (hg19) ; chr5:g.13717422T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717422T>G , CM000667.2:g.13717422T>G	GRCh38
NC_000005.9:g.13717531T>G , CM000667.1:g.13717531T>G	GRCh37
NC_000005.8:g.13770531T>G	NCBI36
NG_013081.1:g.232059A>C
NG_013081.2:g.232059A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12598A>C MANE Select	ENSP00000265104.4:p.Lys4200Gln
ENST00000681290.1:c.12553A>C	ENSP00000505288.1:p.Lys4185Gln
ENST00000265104.4:c.12598A>C	ENSP00000265104.4:p.Lys4200Gln
NM_001369.2:c.12598A>C	NP_001360.1:p.Lys4200Gln
XM_005248262.2:c.12553A>C	XP_005248319.1:p.Lys4185Gln
XM_005248262.3:c.12706A>C	XP_005248319.2:p.Lys4236Gln
XM_017009177.1:c.12706A>C	XP_016864666.1:p.Lys4236Gln
XM_017009178.1:c.11611A>C	XP_016864667.1:p.Lys3871Gln
XM_017009179.2:c.11611A>C	XP_016864668.1:p.Lys3871Gln
XM_017009180.1:c.12706A>C	XP_016864669.1:p.Lys4236Gln
XM_017009185.1:c.7795A>C	XP_016864674.1:p.Lys2599Gln
XM_017009186.1:c.7348A>C	XP_016864675.1:p.Lys2450Gln
XM_017009188.1:c.6685A>C	XP_016864677.1:p.Lys2229Gln
XM_024454388.1:c.11611A>C	XP_024310156.1:p.Lys3871Gln
XM_024454389.1:c.11200A>C	XP_024310157.1:p.Lys3734Gln
NM_001369.3:c.12598A>C MANE Select	NP_001360.1:p.Lys4200Gln