Canonical Allele Identifier: CA8563382

Gene: KRT16

Linked Data

• dbSNP Id: rs773405938
• ExAC: 17:39768948 AG / A
• gnomAD v2: 17-39768948-AG-A
• gnomAD v3: 17-41612696-AG-A
• gnomAD v4: 17-41612696-AG-A
• MyVariant Identifiers: chr17:g.39768949del (hg19) ; chr17:g.41612697del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612698del , CM000679.2:g.41612698del	GRCh38
NC_000017.10:g.39768950del , CM000679.1:g.39768950del	GRCh37
NC_000017.9:g.37022476del	NCBI36
NG_008301.1:g.5131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-9del MANE Select	ENSP00000301653.3:n.-9del
ENST00000301653.8:c.-9del	ENSP00000301653.3:n.-9del
ENST00000588319.1:n.69del
ENST00000590990.1:c.-9del	ENSP00000467105.1:n.-9del
ENST00000593067.1:c.-313+93del	ENSP00000467124.1:n.-313+93del
NM_005557.3:c.-9del	NP_005548.2:n.-9del
NM_005557.4:c.-9del MANE Select	NP_005548.2:n.-9del