Canonical Allele Identifier: CA499998777
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768932G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612680G>C , CM000679.2:g.41612680G>C GRCh38
NC_000017.10:g.39768932G>C , CM000679.1:g.39768932G>C GRCh37
NC_000017.9:g.37022458G>C NCBI36
NG_008301.1:g.5148C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.9C>G MANE Select ENSP00000301653.3:p.Thr3=
ENST00000301653.8:c.9C>G ENSP00000301653.3:p.Thr3=
ENST00000588319.1:n.86C>G
ENST00000590990.1:c.9C>G ENSP00000467105.1:p.Thr3=
ENST00000593067.1:c.-313+110C>G ENSP00000467124.1:n.-313+110C>G
NM_005557.3:c.9C>G NP_005548.2:p.Thr3=
NM_005557.4:c.9C>G MANE Select NP_005548.2:p.Thr3=
Search 100 bp 5'
Search 100 bp 3'