Canonical Allele Identifier: CA399496601
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768835C>A (hg19) chr17:g.41612583C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612583C>A , CM000679.2:g.41612583C>A GRCh38
NC_000017.10:g.39768835C>A , CM000679.1:g.39768835C>A GRCh37
NC_000017.9:g.37022361C>A NCBI36
NG_008301.1:g.5245G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.106G>T MANE Select ENSP00000301653.3:p.Ala36Ser
ENST00000301653.8:c.106G>T ENSP00000301653.3:p.Ala36Ser
ENST00000588319.1:n.183G>T
ENST00000590990.1:c.106G>T ENSP00000467105.1:p.Ala36Ser
ENST00000593067.1:c.-313+207G>T ENSP00000467124.1:n.-313+207G>T
NM_005557.3:c.106G>T NP_005548.2:p.Ala36Ser
NM_005557.4:c.106G>T MANE Select NP_005548.2:p.Ala36Ser
Search 100 bp 5'
Search 100 bp 3'