Canonical Allele Identifier: CA505638222
Gene: KLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.12997877G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887063G>A , CM000681.2:g.12887063G>A GRCh38
NC_000019.9:g.12997877G>A , CM000681.1:g.12997877G>A GRCh37
NC_000019.8:g.12858877G>A NCBI36
NG_009292.1:g.904G>A
NG_013087.1:g.5141C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.78C>T MANE Select ENSP00000264834.3:p.Asp26=
ENST00000264834.4:c.78C>T ENSP00000264834.3:p.Asp26=
NM_006563.3:c.78C>T NP_006554.1:p.Asp26=
XM_011527642.1:c.-126C>T XP_011525944.1:n.-126C>T
NM_006563.4:c.78C>T NP_006554.1:p.Asp26=
XM_011527642.2:c.-126C>T XP_011525944.1:n.-126C>T
NM_006563.5:c.78C>T MANE Select NP_006554.1:p.Asp26=