Canonical Allele Identifier: CA375426067
Gene: SARDH HGNC NCBI

Linked Data

dbSNP Id: rs137999690

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133729791C>G , CM000671.2:g.133729791C>G GRCh38
NC_000009.11:g.136594913C>G , CM000671.1:g.136594913C>G GRCh37
NC_000009.10:g.135584734C>G NCBI36
NG_008987.1:g.15165G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439388.6:c.889G>C MANE Select ENSP00000403084.1:p.Val297Leu
ENST00000298628.6:c.889G>C ENSP00000298628.5:p.Val297Leu
ENST00000371867.5:c.622G>C ENSP00000360933.1:p.Val208Leu
ENST00000371872.8:c.889G>C ENSP00000360938.4:p.Val297Leu
ENST00000422262.6:c.49G>C ENSP00000415537.3:p.Val17Leu
ENST00000427237.6:c.889G>C ENSP00000394210.2:p.Val297Leu
ENST00000439388.5:c.889G>C ENSP00000403084.1:p.Val297Leu
ENST00000616662.4:c.889G>C ENSP00000484683.1:p.Val297Leu
NM_001134707.1:c.889G>C NP_001128179.1:p.Val297Leu
NM_007101.3:c.889G>C NP_009032.2:p.Val297Leu
XM_006716990.2:c.889G>C XP_006717053.1:p.Val297Leu
XM_011518333.1:c.889G>C XP_011516635.1:p.Val297Leu
XR_929726.1:n.1056G>C
XR_929727.1:n.1056G>C
XR_929728.1:n.1056G>C
XM_017014367.1:c.889G>C XP_016869856.1:p.Val297Leu
XM_017014368.1:c.889G>C XP_016869857.1:p.Val297Leu
XR_001746213.1:n.1185G>C
XR_001746214.1:n.2368G>C
XR_001746215.1:n.1187G>C
XR_001746216.1:n.1185G>C
XR_001746217.1:n.1185G>C
XR_001746218.1:n.1185G>C
XR_929726.2:n.1056G>C
NM_001134707.2:c.889G>C MANE Select NP_001128179.1:p.Val297Leu
NM_007101.4:c.889G>C NP_009032.2:p.Val297Leu