Canonical Allele Identifier: CA505638438
Gene: KLF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.12997925G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12887111G>C , CM000681.2:g.12887111G>C GRCh38
NC_000019.9:g.12997925G>C , CM000681.1:g.12997925G>C GRCh37
NC_000019.8:g.12858925G>C NCBI36
NG_009292.1:g.952G>C
NG_013087.1:g.5093C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264834.6:c.30C>G MANE Select ENSP00000264834.3:p.Ser10=
ENST00000264834.4:c.30C>G ENSP00000264834.3:p.Ser10=
NM_006563.3:c.30C>G NP_006554.1:p.Ser10=
XM_011527642.1:c.-174C>G XP_011525944.1:n.-174C>G
NM_006563.4:c.30C>G NP_006554.1:p.Ser10=
XM_011527642.2:c.-174C>G XP_011525944.1:n.-174C>G
NM_006563.5:c.30C>G MANE Select NP_006554.1:p.Ser10=
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