Canonical Allele Identifier: CA505638428
Gene: KLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.12997922G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887108G>T , CM000681.2:g.12887108G>T GRCh38
NC_000019.9:g.12997922G>T , CM000681.1:g.12997922G>T GRCh37
NC_000019.8:g.12858922G>T NCBI36
NG_009292.1:g.949G>T
NG_013087.1:g.5096C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.33C>A MANE Select ENSP00000264834.3:p.Ile11=
ENST00000264834.4:c.33C>A ENSP00000264834.3:p.Ile11=
NM_006563.3:c.33C>A NP_006554.1:p.Ile11=
XM_011527642.1:c.-171C>A XP_011525944.1:n.-171C>A
NM_006563.4:c.33C>A NP_006554.1:p.Ile11=
XM_011527642.2:c.-171C>A XP_011525944.1:n.-171C>A
NM_006563.5:c.33C>A MANE Select NP_006554.1:p.Ile11=