Canonical Allele Identifier: CA505638367
Gene: KLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.12997907G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887093G>C , CM000681.2:g.12887093G>C GRCh38
NC_000019.9:g.12997907G>C , CM000681.1:g.12997907G>C GRCh37
NC_000019.8:g.12858907G>C NCBI36
NG_009292.1:g.934G>C
NG_013087.1:g.5111C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.48C>G MANE Select ENSP00000264834.3:p.Ala16=
ENST00000264834.4:c.48C>G ENSP00000264834.3:p.Ala16=
NM_006563.3:c.48C>G NP_006554.1:p.Ala16=
XM_011527642.1:c.-156C>G XP_011525944.1:n.-156C>G
NM_006563.4:c.48C>G NP_006554.1:p.Ala16=
XM_011527642.2:c.-156C>G XP_011525944.1:n.-156C>G
NM_006563.5:c.48C>G MANE Select NP_006554.1:p.Ala16=