Canonical Allele Identifier: CA372291933

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584676C>G (hg19) ; chr8:g.132572428C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572428C>G , CM000670.2:g.132572428C>G	GRCh38
NC_000008.10:g.133584676C>G , CM000670.1:g.133584676C>G	GRCh37
NC_000008.9:g.133653858C>G	NCBI36
NG_033068.1:g.108188G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1279G>C MANE Select	ENSP00000484634.1:p.Asp427His
ENST00000250173.5:c.*143G>C	ENSP00000250173.2:n.*143G>C
ENST00000518642.5:c.*143G>C	ENSP00000428610.1:n.*143G>C
ENST00000519595.5:c.1279G>C	ENSP00000429791.1:p.Asp427His
ENST00000522597.1:n.548G>C
ENST00000522789.5:c.499G>C	ENSP00000428015.1:p.Asp167His
ENST00000618342.1:c.1279G>C	ENSP00000484802.1:p.Asp427His
ENST00000620350.4:c.1279G>C	ENSP00000484634.1:p.Asp427His
NM_012472.4:c.1279G>C	NP_036604.2:p.Asp427His
NR_073525.1:n.1503G>C
XM_006716538.2:c.1297G>C	XP_006716601.2:p.Asp433His
XM_011516950.1:c.1237G>C	XP_011515252.1:p.Asp413His
XM_011516952.1:c.1033G>C	XP_011515254.1:p.Asp345His
XM_011516953.1:c.919G>C	XP_011515255.1:p.Asp307His
XM_011516954.1:c.919G>C	XP_011515256.1:p.Asp307His
XR_428377.2:n.1531G>C
NM_001321961.1:c.1219G>C	NP_001308890.1:p.Asp407His
NM_001321962.1:c.1033G>C	NP_001308891.1:p.Asp345His
NM_001321963.1:c.919G>C	NP_001308892.1:p.Asp307His
NM_001321964.1:c.919G>C	NP_001308893.1:p.Asp307His
NM_001321965.1:c.919G>C	NP_001308894.1:p.Asp307His
NM_001321966.1:c.859G>C	NP_001308895.1:p.Asp287His
NM_012472.5:c.1279G>C	NP_036604.2:p.Asp427His
NR_073525.2:n.1503G>C
NR_135905.1:n.1492G>C
NR_135906.1:n.933G>C
NR_135907.1:n.1179G>C
NR_135908.1:n.873G>C
NR_135909.1:n.1297G>C
NR_135910.1:n.1604G>C
NR_135911.1:n.1683G>C
NR_135912.1:n.2242G>C
NR_135913.1:n.1929G>C
XM_006716538.3:c.1297G>C	XP_006716601.2:p.Asp433His
XM_011516950.2:c.1237G>C	XP_011515252.1:p.Asp413His
XM_017013296.1:c.1177G>C	XP_016868785.1:p.Asp393His
XM_017013297.1:c.919G>C	XP_016868786.1:p.Asp307His
XM_017013298.1:c.919G>C	XP_016868787.1:p.Asp307His
NM_012472.6:c.1279G>C MANE Select	NP_036604.2:p.Asp427His
NM_001321961.2:c.1219G>C	NP_001308890.1:p.Asp407His
NM_001321962.2:c.1033G>C	NP_001308891.1:p.Asp345His
NM_001321963.2:c.919G>C	NP_001308892.1:p.Asp307His
NM_001321964.2:c.919G>C	NP_001308893.1:p.Asp307His
NM_001321965.2:c.919G>C	NP_001308894.1:p.Asp307His
NM_001321966.2:c.859G>C	NP_001308895.1:p.Asp287His
NR_073525.3:n.1431G>C
NR_135905.2:n.1420G>C
NR_135906.2:n.861G>C
NR_135907.2:n.1107G>C
NR_135908.2:n.801G>C
NR_135909.2:n.1317G>C
NR_135910.2:n.1667G>C
NR_135911.2:n.1787G>C
NR_135912.2:n.2346G>C
NR_135913.2:n.2033G>C