Canonical Allele Identifier: CA467620400

Gene: SARDH

Linked Data

• MyVariant Identifiers: chr9:g.136594971A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133729849A>C , CM000671.2:g.133729849A>C	GRCh38
NC_000009.11:g.136594971A>C , CM000671.1:g.136594971A>C	GRCh37
NC_000009.10:g.135584792A>C	NCBI36
NG_008987.1:g.15107T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439388.6:c.831T>G MANE Select	ENSP00000403084.1:p.Ala277=
ENST00000298628.6:c.831T>G	ENSP00000298628.5:p.Ala277=
ENST00000371867.5:c.564T>G	ENSP00000360933.1:p.Ala188=
ENST00000371872.8:c.831T>G	ENSP00000360938.4:p.Ala277=
ENST00000422262.6:c.-10T>G	ENSP00000415537.3:n.-10T>G
ENST00000427237.6:c.831T>G	ENSP00000394210.2:p.Ala277=
ENST00000439388.5:c.831T>G	ENSP00000403084.1:p.Ala277=
ENST00000616662.4:c.831T>G	ENSP00000484683.1:p.Ala277=
NM_001134707.1:c.831T>G	NP_001128179.1:p.Ala277=
NM_007101.3:c.831T>G	NP_009032.2:p.Ala277=
XM_006716990.2:c.831T>G	XP_006717053.1:p.Ala277=
XM_011518333.1:c.831T>G	XP_011516635.1:p.Ala277=
XR_929726.1:n.998T>G
XR_929727.1:n.998T>G
XR_929728.1:n.998T>G
XM_017014367.1:c.831T>G	XP_016869856.1:p.Ala277=
XM_017014368.1:c.831T>G	XP_016869857.1:p.Ala277=
XR_001746213.1:n.1127T>G
XR_001746214.1:n.2310T>G
XR_001746215.1:n.1129T>G
XR_001746216.1:n.1127T>G
XR_001746217.1:n.1127T>G
XR_001746218.1:n.1127T>G
XR_929726.2:n.998T>G
NM_001134707.2:c.831T>G MANE Select	NP_001128179.1:p.Ala277=
NM_007101.4:c.831T>G	NP_009032.2:p.Ala277=