Canonical Allele Identifier: CA4881325

Gene: DNAAF11

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132625455C>A , CM000670.2:g.132625455C>A	GRCh38
NC_000008.10:g.133637701C>A , CM000670.1:g.133637701C>A	GRCh37
NC_000008.9:g.133706883C>A	NCBI36
NG_033068.1:g.55163G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012472.6:c.654-1G>T MANE Select	NP_036604.2:n.654-1G>T
ENST00000620350.5:c.654-1G>T MANE Select	ENSP00000484634.1:n.654-1G>T
NM_001321961.1:c.654-1G>T	NP_001308890.1:n.654-1G>T
NM_001321961.2:c.654-1G>T	NP_001308890.1:n.654-1G>T
NM_001321962.1:c.408-1G>T	NP_001308891.1:n.408-1G>T
NM_001321962.2:c.408-1G>T	NP_001308891.1:n.408-1G>T
NM_001321963.1:c.294-1G>T	NP_001308892.1:n.294-1G>T
NM_001321963.2:c.294-1G>T	NP_001308892.1:n.294-1G>T
NM_001321964.1:c.294-1G>T	NP_001308893.1:n.294-1G>T
NM_001321964.2:c.294-1G>T	NP_001308893.1:n.294-1G>T
NM_001321965.1:c.294-1G>T	NP_001308894.1:n.294-1G>T
NM_001321965.2:c.294-1G>T	NP_001308894.1:n.294-1G>T
NM_001321966.1:c.294-1G>T	NP_001308895.1:n.294-1G>T
NM_001321966.2:c.294-1G>T	NP_001308895.1:n.294-1G>T
NM_012472.4:c.654-1G>T	NP_036604.2:n.654-1G>T
NM_012472.5:c.654-1G>T	NP_036604.2:n.654-1G>T
NR_073525.1:n.778-1G>T
NR_073525.2:n.778-1G>T
NR_073525.3:n.706-1G>T
NR_135905.1:n.867-1G>T
NR_135905.2:n.795-1G>T
NR_135906.1:n.308-1G>T
NR_135906.2:n.236-1G>T
NR_135907.1:n.554-1G>T
NR_135907.2:n.482-1G>T
NR_135908.1:n.308-1G>T
NR_135908.2:n.236-1G>T
NR_135909.1:n.672-1G>T
NR_135909.2:n.692-1G>T
NR_135910.1:n.979-1G>T
NR_135910.2:n.1042-1G>T
NR_135911.1:n.1058-1G>T
NR_135911.2:n.1162-1G>T
NR_135912.1:n.1617-1G>T
NR_135912.2:n.1721-1G>T
NR_135913.1:n.1304-1G>T
NR_135913.2:n.1408-1G>T
ENST00000250173.5:c.654-1G>T	ENSP00000250173.2:n.654-1G>T
ENST00000518642.5:c.654-1G>T	ENSP00000428610.1:n.654-1G>T
ENST00000519595.5:c.654-1G>T	ENSP00000429791.1:n.654-1G>T
ENST00000520446.5:n.529-1G>T
ENST00000523503.1:n.416-1G>T
ENST00000618342.1:c.654-1G>T	ENSP00000484802.1:n.654-1G>T
ENST00000620350.4:c.654-1G>T	ENSP00000484634.1:n.654-1G>T
XM_006716538.2:c.672-1G>T	XP_006716601.2:n.672-1G>T
XM_006716538.3:c.672-1G>T	XP_006716601.2:n.672-1G>T
XM_011516950.1:c.672-1G>T	XP_011515252.1:n.672-1G>T
XM_011516950.2:c.672-1G>T	XP_011515252.1:n.672-1G>T
XM_011516951.1:c.672-1G>T	XP_011515253.1:n.672-1G>T
XM_011516952.1:c.408-1G>T	XP_011515254.1:n.408-1G>T
XM_011516953.1:c.294-1G>T	XP_011515255.1:n.294-1G>T
XM_011516954.1:c.294-1G>T	XP_011515256.1:n.294-1G>T
XM_017013296.1:c.552-1G>T	XP_016868785.1:n.552-1G>T
XM_017013297.1:c.294-1G>T	XP_016868786.1:n.294-1G>T
XM_017013298.1:c.294-1G>T	XP_016868787.1:n.294-1G>T
XR_428377.2:n.797-1G>T